Item 33 of 82 (back to results) previous next   Diethylhexyl Phthalate D004051               MeSH Unique Identifier: D004051 Scope Notes: An ester of phthalic acid. It appears as a light-colored, odorless liquid and is used as a plasticizer for many resins and elastomers. Chemical – Gene Interaction Note 1: Diethylhexyl Phthalate promotes the reaction [NR1I2 protein results in increased expression of ABCB1 mRNA] Note 2: Diethylhexyl Phthalate results in increased expression of ABCB1 mRNA Click here for more information

Current search: C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140] > Bone Diseases [MESH:D001847] > Bone Diseases, Metabolic [MESH:D001851] > Pseudohypoparathyroidism [MESH:D011547] > Pseudohypoparathyroidism Type 1B [MESH:C548075] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily B [HGNC:ABCB] (452)   ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355)  Basic helix-loop-helix [HGNC:BHLH] (618)   nuclear receptor coactivator 1 [HGNC:NCOA1] (71)  v-myc avian myelocytomatosis viral oncogene homolog [HGNC:MYC] (254)  CD molecules [HGNC:CD] (1459)   ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355)  lysosomal-associated membrane protein 3 [HGNC:LAMP3] (37)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566)  cytochrome P450, family 01, subfamily B, polypeptide 01 [HGNC:CYP1B1] (301)  cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 04 [HGNC:IL4] (164)  K-acetyltransferases [HGNC:KAT] (176)   nuclear receptor coactivator 1 [HGNC:NCOA1] (71)  Mitogen-activated protein kinase cascade [HGNC:MAP#K] (854)   Mitogen-activated protein kinases [HGNC:MAPK] (797)   mitogen-activated protein kinase 01 [HGNC:MAPK1] (651)  mitogen-activated protein kinase 03 [HGNC:MAPK3] (644)  Nuclear hormone receptors [HGNC:NR] (1322)   estrogen receptor 1 [HGNC:ESR1] (506)  estrogen receptor 2 (ER beta) [HGNC:ESR2] (261)  nuclear receptor subfamily 1, group I, member 2 [HGNC:NR1I2] (328)  nuclear receptor subfamily 1, group I, member 3 [HGNC:NR1I3] (123)  peroxisome proliferator-activated receptor alpha [HGNC:PPARA] (156)  peroxisome proliferator-activated receptor delta [HGNC:PPARD] (67)  Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898)   tumor necrosis factor [HGNC:TNF] (795) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  cotreatment (1499)  response to substance (623)  Decreases (5154)   activity (2549)  expression (2187)  reaction (3393)  response to substance (713)  Increases (5571)   activity (2865)  expression (3238)  phosphorylation (1060)  reaction (1574)  secretion (901) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Lower Extremity [MESH:D035002] (139)   Foot [MESH:D005528] (125)   Forefoot, Human [MESH:D005545] (118)   Toes [MESH:D014034] (115)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Syndactyly, type 3 [MESH:C538154] (192)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Meier-Gorlin syndrome [MESH:C538012] (133)  Face [MESH:D005145] (387)   Coffin-Siris syndrome [MESH:C536436] (102)  Frontonasal dysplasia [MESH:C538065] (52)  Mouth [MESH:D009055] (40)   Lip [MESH:D008046] (39)   Van der Woude syndrome [MESH:C536528] (33)  Nose [MESH:D009666] (71)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Neck [MESH:D009333] (107)   Coffin-Siris syndrome [MESH:C536436] (102)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Leg Bones [MESH:D007867] (228)   Patella [MESH:D010329] (168)   Meier-Gorlin syndrome [MESH:C538012] (133)  Skull [MESH:D012886] (610)   Facial Bones [MESH:D005147] (539)   Jaw [MESH:D007568] (524)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Sphenoid Bone [MESH:D013100] (19)   Sella Turcica [MESH:D012658] (18)   Pituitary Hormone Deficiency, Combined, 4 [MESH:C567492] (15)  Thorax [MESH:D013909] (62)   Ribs [MESH:D012272] (50)   Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Joints [MESH:D007596] (126)   Knee Joint [MESH:D007719] (38)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Respiratory System [MESH:D012137] (321)   Nose [MESH:D009666] (91)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Urogenital System [MESH:D014566] (986)   Genitalia [MESH:D005835] (400)   Genitalia, Male [MESH:D005837] (297)   Testis [MESH:D013737] (92)   Leydig Cell Hypoplasia [MESH:C562567] (65)  Gonads [MESH:D006066] (91)   Testis [MESH:D013737] (86)   Leydig Cell Hypoplasia [MESH:C562567] (65)  Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   Nephrons [MESH:D009399] (518)   Kidney Tubules [MESH:D007684] (510)   Kidney Tubules, Proximal [MESH:D007687] (504)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Endocrine System [MESH:D004703] (206)   Endocrine Glands [MESH:D004702] (193)   Gonads [MESH:D006066] (99)   Testis [MESH:D013737] (87)   Leydig Cell Hypoplasia [MESH:C562567] (65)  Thyroid Gland [MESH:D013961] (53)   Thyroid Dyshormonogenesis 3 [MESH:C562769] (46)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Conduction System [MESH:D006329] (263)   Short QT Syndrome 3 [MESH:C566504] (39)  Short QT Syndrome 2 [MESH:C566505] (45)  Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Meier-Gorlin syndrome [MESH:C538012] (133)  Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Peters anomaly [MESH:C537884] (465)  Nose [MESH:D009666] (74)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Cells [MESH:D002477] (1885)   Blood Cells [MESH:D001773] (196)   Erythrocytes [MESH:D004912] (146)   Erythrocytes, Abnormal [MESH:D004913] (141)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127)  Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 21-22 and Y [MESH:D002904] (294)   Chromosomes, Human, Pair 22 [MESH:D002892] (250)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Inclusion Bodies [MESH:D002479] (147)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127)  Stomatognathic System [MESH:D013284] (673)   Jaw [MESH:D007568] (528)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Mouth [MESH:D009055] (194)   Lip [MESH:D008046] (42)   Van der Woude syndrome [MESH:C536528] (33)  Hemic and Immune Systems [MESH:D006424] (272)   Blood [MESH:D001769] (200)   Blood Cells [MESH:D001773] (194)   Erythrocytes [MESH:D004912] (146)   Erythrocytes, Abnormal [MESH:D004913] (141)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Central Nervous System Bacterial Infections [MESH:D020806] (141)   Meningitis, Bacterial [MESH:D016920] (128)   Meningitis, Meningococcal [MESH:D008585] (81)  Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Pasteurellaceae Infections [MESH:D016871] (348)  Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Enterobacteriaceae Infections [MESH:D004756] (669)   Salmonella Infections [MESH:D012480] (620)   Salmonella Infections, Animal [MESH:D012481] (604)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Neisseriaceae Infections [MESH:D016870] (273)   Meningococcal Infections [MESH:D008589] (242)   Meningitis, Meningococcal [MESH:D008585] (81)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Staphylococcal Infections [MESH:D013203] (264)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)   Atypical Mycobacteriosis, Familial, X-Linked 1 [MESH:C567070] (56)  Tuberculosis [MESH:D014376] (992)   Tuberculosis, Bovine [MESH:D014380] (380)  Streptococcal Infections [MESH:D013290] (158)   Pneumococcal Infections [MESH:D011008] (122)   Invasive Pneumococcal Disease, Recurrent Isolated, 2 [MESH:C564468] (56)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Bone Diseases, Infectious [MESH:D001850] (90)   Osteomyelitis [MESH:D010019] (69)   Majeed syndrome [MESH:C537839] (33)  Intraabdominal Infections [MESH:D059413] (958)   Appendicitis [MESH:D001064] (774)  Peritonitis [MESH:D010538] (800)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Papillomavirus Infections [MESH:D030361] (630)  Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Slow Virus Diseases [MESH:D012897] (782)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  Tumor Virus Infections [MESH:D014412] (1069)   Papillomavirus Infections [MESH:D030361] (537)  Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   Nematode Infections [MESH:D009349] (870)   Adenophorea Infections [MESH:D017188] (808)   Enoplida Infections [MESH:D017189] (807)   Trichuriasis [MESH:D014257] (805)  Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Protozoan Infections [MESH:D011528] (3014)   Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Visceral [MESH:D007898] (2149)  Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Malaria [MESH:D008288] (2175)   Malaria, Falciparum [MESH:D016778] (438)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Radiation-Induced [MESH:D009381] (174)  Neoplasms, Second Primary [MESH:D016609] (518)  Cysts [MESH:D003560] (2625)   Van der Woude syndrome [MESH:C536528] (33)  Follicular Cyst [MESH:D005497] (151)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Monocytic, Acute [MESH:D007948] (98)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Extranodal NK-T-Cell [MESH:D054391] (132)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Hepatoblastoma [MESH:D018197] (548)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Neoplasms, Adipose Tissue [MESH:D018205] (677)   Liposarcoma [MESH:D008080] (612)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Chondroma [MESH:D002812] (155)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Solitary Fibrous Tumors [MESH:D054364] (79)  Fibroma [MESH:D005350] (1578)   Fibromatosis, Aggressive [MESH:D018222] (1562)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Smooth Muscle Tumor [MESH:D018235] (132)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Liposarcoma [MESH:D008080] (612)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Ependymoma [MESH:D004806] (76)  Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)   Uveal melanoma [MESH:C536494] (109)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Hepatic Adenomas, Familial [MESH:C564190] (49)  ACTH-Secreting Pituitary Adenoma [MESH:D049913] (169)  Adenoma, Liver Cell [MESH:D018248] (685)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Mesothelioma [MESH:D008654] (2567)  Prolactinoma [MESH:D015175] (312)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Pilomatrixoma [MESH:D018296] (252)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Ependymoma [MESH:D004806] (76)  Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Gonadal Tissue [MESH:D018309] (284)   Sex Cord-Gonadal Stromal Tumors [MESH:D018312] (282)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Nerve Sheath Neoplasms [MESH:D018317] (365)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Ependymoma [MESH:D004806] (76)  Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)   Uveal melanoma [MESH:C536494] (109)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioblastoma [MESH:D018325] (395)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Nevus [MESH:D009506] (340)  Melanoma [MESH:D008545] (3508)   Uveal melanoma [MESH:C536494] (109)  Neoplasms by Site [MESH:D009371] (9169)   Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Hepatic Adenomas, Familial [MESH:C564190] (49)  Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroid cancer, Hurthle cell [MESH:C536913] (24)  Eye Neoplasms [MESH:D005134] (400)   Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Nose Neoplasms [MESH:D009669] (390)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroid cancer, Hurthle cell [MESH:C536913] (24)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Thymus Neoplasms [MESH:D013953] (247)  Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Tuberous Sclerosis [MESH:D014402] (635)  Wilms Tumor [MESH:D009396] (553)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Precancerous Conditions [MESH:D011230] (2858)   Aberrant Crypt Foci [MESH:D058739] (326)  Xeroderma Pigmentosum [MESH:D014983] (213)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Cartilage Diseases [MESH:D002357] (438)  Bone Diseases [MESH:D001847] (5801)   Osteonecrosis [MESH:D010020] (539)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromicric dysplasia [MESH:C535662] (520)  Marfan Syndrome [MESH:D008382] (646)  Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Hajdu-Cheney Syndrome [MESH:D031845] (42)  Dwarfism [MESH:D004392] (778)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 4 [MESH:C567492] (15)  Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Gigantism [MESH:D005877] (46)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Osteochondrodysplasias [MESH:D010009] (2440)   Jansen type metaphyseal chondrodysplasia [MESH:C537564] (40)  Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Eiken Skeletal Dysplasia [MESH:C564010] (40)  Spondyloepimetaphyseal Dysplasia, Pakistani Type [MESH:C567551] (63)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Cleidocranial Dysplasia [MESH:D002973] (129)  Enchondromatosis [MESH:D004687] (170)  Langer-Giedion Syndrome [MESH:D015826] (25)  Fibrous Dysplasia of Bone [MESH:D005357] (737)   Fibrous Dysplasia, Polyostotic [MESH:D005359] (82)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Osteosclerosis [MESH:D010026] (356)   Osteopetrosis [MESH:D010022] (318)   Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Bone Diseases, Endocrine [MESH:D001849] (747)   Acromegaly [MESH:D000172] (466)  Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 4 [MESH:C567492] (15)  Gigantism [MESH:D005877] (46)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Bone Diseases, Infectious [MESH:D001850] (90)   Osteomyelitis [MESH:D010019] (69)   Majeed syndrome [MESH:C537839] (33)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Bone Resorption [MESH:D001862] (2352)   Alveolar Bone Loss [MESH:D016301] (220)  Osteolysis [MESH:D010014] (1787)   Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Hajdu-Cheney Syndrome [MESH:D031845] (42)  Hyperostosis [MESH:D015576] (493)   Exostoses [MESH:D005096] (160)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)   Intervertebral disc disease [MESH:C535531] (514)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Eiken Skeletal Dysplasia [MESH:C564010] (40)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Coffin-Siris syndrome [MESH:C536436] (102)  Eiken Skeletal Dysplasia [MESH:C564010] (40)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Jaw Diseases [MESH:D007571] (1601)   Mandibular Diseases [MESH:D008336] (395)  Maxillary Diseases [MESH:D008439] (354)  Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Joint Diseases [MESH:D007592] (4657)   Ankylosis [MESH:D000844] (479)   Spondylitis, Ankylosing [MESH:D013167] (431)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Gout [MESH:D006073] (261)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Arthrogryposis [MESH:D001176] (329)   Distal arthrogryposis type 2B [MESH:C538400] (85)  Muscular Diseases [MESH:D009135] (4071)   VLCAD deficiency [MESH:C536353] (55)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Muscle Spasticity [MESH:D009128] (187)  Muscle Weakness [MESH:D018908] (478)  Arthrogryposis [MESH:D001176] (329)   Distal arthrogryposis type 2B [MESH:C538400] (85)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency [MESH:C567709] (41)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 3 [MESH:C538350] (70)  Nemaline myopathy 4 [MESH:C538351] (47)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Myotonic Disorders [MESH:D020967] (138)   Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Rhabdomyolysis [MESH:D012206] (465)   Myoglobinuria [MESH:D009212] (96)   Myoglobinuria, Acute Recurrent, Autosomal Recessive [MESH:C564832] (64)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Arthrogryposis [MESH:D001176] (329)   Distal arthrogryposis type 2B [MESH:C538400] (85)  Craniofacial Abnormalities [MESH:D019465] (3098)   Frontonasal dysplasia [MESH:C538065] (52)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Cleidocranial Dysplasia [MESH:D002973] (129)  Craniosynostoses [MESH:D003398] (438)  Donohue Syndrome [MESH:D056731] (95)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Microcephaly [MESH:D008831] (700)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Split-Hand/Foot Malformation 6 [MESH:C567616] (29)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Brachydactyly [MESH:D059327] (220)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Foot Deformities, Congenital [MESH:D005532] (538)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Eiken Skeletal Dysplasia [MESH:C564010] (40)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Coffin-Siris syndrome [MESH:C536436] (102)  Eiken Skeletal Dysplasia [MESH:C564010] (40)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Gout [MESH:D006073] (261)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Bile Duct Neoplasms [MESH:D001650] (367)  Cholangitis [MESH:D002761] (203)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Cholestasis, progressive familial intrahepatic 2 [MESH:C535934] (190)  Cholestasis, progressive familial intrahepatic 3 [MESH:C535935] (101)  Alagille Syndrome [MESH:D016738] (105)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Cholelithiasis [MESH:D002769] (373)   Gallstones [MESH:D042882] (350)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Cholecystolithiasis [MESH:D041761] (353)   Gallstones [MESH:D042882] (350)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Hirschsprung Disease [MESH:D006627] (361)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Hepatic Adenomas, Familial [MESH:C564190] (49)  Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Stenosis [MESH:D004940] (490)  Esophagitis [MESH:D004941] (1120)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Gastroenteritis [MESH:D005759] (4066)   Appendicitis [MESH:D001064] (774)  Esophagitis [MESH:D004941] (1120)  Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 14 [MESH:C567383] (22)  Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Appendicitis [MESH:D001064] (774)  Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colonic Diseases, Functional [MESH:D003109] (439)   Irritable Bowel Syndrome [MESH:D043183] (429)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 14 [MESH:C567383] (22)  Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Zellweger Syndrome [MESH:D015211] (182)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Cholestasis, progressive familial intrahepatic 2 [MESH:C535934] (190)  Cholestasis, progressive familial intrahepatic 3 [MESH:C535935] (101)  Alagille Syndrome [MESH:D016738] (105)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   End Stage Liver Disease [MESH:D058625] (108)  Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Hepatitis, Animal [MESH:D006520] (260)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis C, Chronic [MESH:D019698] (142)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Hepatic Adenomas, Familial [MESH:C564190] (49)  Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Congenital Hyperinsulinism [MESH:D044903] (132)  Cystic Fibrosis [MESH:D003550] (760)  Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Peritoneal Diseases [MESH:D010532] (1119)   Peritoneal Fibrosis [MESH:D056627] (488)  Peritonitis [MESH:D010538] (800) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Mandibular Diseases [MESH:D008336] (450)  Maxillary Diseases [MESH:D008439] (354)  Jaw Abnormalities [MESH:D007569] (1435)   External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation [MESH:C566509] (71)  Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  PCI 5002 [MESH:C568608] (527)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Oral Ulcer [MESH:D019226] (488)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Orofacial Cleft 11 [MESH:C567410] (101)  PCI 5002 [MESH:C568608] (433)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Orofacial Cleft 11 [MESH:C567410] (101)  PCI 5002 [MESH:C568608] (433)  Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Periodontal Diseases [MESH:D010510] (1001)   Poikiloderma of Kindler [MESH:C536321] (64)  Periodontal Atrophy [MESH:D055093] (225)   Alveolar Bone Loss [MESH:D016301] (220)  Periodontitis [MESH:D010518] (843)   Periodontitis, Aggressive, 2 [MESH:C566946] (310)  Aggressive Periodontitis [MESH:D010520] (74)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Hypoglossia, Isolated [MESH:C567568] (57)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation [MESH:C566509] (71)  Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Orofacial Cleft 11 [MESH:C567410] (101)  Orofacial Cleft 12 [MESH:C567548] (434)  Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Tooth Agenesis, Selective, 6 [MESH:C567755] (154)  Anodontia [MESH:D000848] (185)   Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism [MESH:C567313] (18)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Hypomaturation Type, Iia3 [MESH:C567706] (22)  Tooth Diseases [MESH:D014076] (742)   Failure of Tooth Eruption, Primary [MESH:C565114] (41)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Tooth Agenesis, Selective, 6 [MESH:C567755] (154)  Anodontia [MESH:D000848] (185)   Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism [MESH:C567313] (18)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Hypomaturation Type, Iia3 [MESH:C567706] (22) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Respiratory System Abnormalities [MESH:D015619] (243)  Bronchial Diseases [MESH:D001982] (4382)   Bronchial Hyperreactivity [MESH:D016535] (1357)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Bronchiectasis [MESH:D001987] (1792)   Bronchiectasis With Or Without Elevated Sweat Chloride 2 [MESH:C567813] (77)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Hypertension, Pulmonary [MESH:D006976] (2000)  Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Alveolitis, Extrinsic Allergic [MESH:D000542] (496)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Rhinitis [MESH:D012220] (1134)  Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Hyperventilation [MESH:D006985] (654)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Obstructive [MESH:D020181] (126)  Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Insufficiency [MESH:D012131] (841)   Hypoventilation [MESH:D007040] (360)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Nose Neoplasms [MESH:D009669] (390)  Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 31 [MESH:C564629] (13)  Deafness, Autosomal Dominant 20 [MESH:C565754] (69)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Rhinitis [MESH:D012220] (1134)  Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Nose Neoplasms [MESH:D009669] (390)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Chronobiology Disorders [MESH:D021081] (970)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Autonomic Nervous System Diseases [MESH:D001342] (882)   dopamine beta hydroxylase deficiency [MESH:C535600] (63)  Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)   Hypotension, Orthostatic [MESH:D007024] (679)  Central Nervous System Diseases [MESH:D002493] (9745)   Meningitis [MESH:D008581] (352)  Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Huntington Disease [MESH:D006816] (540)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency [MESH:C566449] (24)  Hepatic Encephalopathy [MESH:D006501] (1795)  Kernicterus [MESH:D007647] (256)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Galactosemias [MESH:D005693] (69)  Homocystinuria [MESH:D006712] (93)  Leigh Disease [MESH:D007888] (206)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Maple Syrup Urine Disease [MESH:D008375] (127)  Tyrosinemias [MESH:D020176] (132)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Canavan Disease [MESH:D017825] (29)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Peroxisomal Disorders [MESH:D018901] (1472)   Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Hypoxia-Ischemia, Brain [MESH:D020925] (33)   Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency [MESH:C566449] (24)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Huntington Disease [MESH:D006816] (540)  Lewy Body Disease [MESH:D020961] (1143)  Epilepsy [MESH:D004827] (6274)   Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Frontal Lobe [MESH:D017034] (172)   Epilepsy, Nocturnal Frontal Lobe, Type 4 [MESH:C563679] (43)  Epilepsy, Generalized [MESH:D004829] (1431)   Generalized Epilepsy and Paroxysmal Dyskinesia [MESH:C563719] (51)  Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Spasms, Infantile [MESH:D013036] (468)  Seizures [MESH:D012640] (4502)   Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency [MESH:C566449] (24)  Seizures, Febrile [MESH:D003294] (229)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)   Migraine without Aura [MESH:D020326] (408)  Hypothalamic Diseases [MESH:D007027] (1833)   Bardet-Biedl Syndrome [MESH:D020788] (110)  Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Hyperpituitarism [MESH:D006964] (1250)   Acromegaly [MESH:D000172] (466)  Hyperprolactinemia [MESH:D006966] (603)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Hypopituitarism [MESH:D007018] (732)   Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 4 [MESH:C567492] (15)  Inappropriate ADH Syndrome [MESH:D007177] (178)   Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Hypoxia, Brain [MESH:D002534] (134)   Hypoxia-Ischemia, Brain [MESH:D020925] (33)   Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency [MESH:C566449] (24)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Canavan Disease [MESH:D017825] (29)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Bacterial Infections [MESH:D020806] (147)   Meningitis, Bacterial [MESH:D016920] (128)   Meningitis, Meningococcal [MESH:D008585] (81)  Meningitis [MESH:D008581] (1506)   Meningitis, Bacterial [MESH:D016920] (128)   Meningitis, Meningococcal [MESH:D008585] (81)  Prion Diseases [MESH:D017096] (488)   Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Tic Disorders [MESH:D013981] (256)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Paroxysmal nonkinesigenic dyskinesia [MESH:C537181] (23)  Generalized Epilepsy and Paroxysmal Dyskinesia [MESH:C563719] (51)  Huntington Disease [MESH:D006816] (540)  Dystonic Disorders [MESH:D020821] (729)   Segawa syndrome, autosomal recessive [MESH:C537537] (220)  Juvenile-onset dystonia [MESH:C537704] (143)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Ocular Motility Disorders [MESH:D015835] (364)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Multiple Sclerosis [MESH:D009103] (1716)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Canavan Disease [MESH:D017825] (29)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Nervous System Malformations [MESH:D009421] (3354)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)  Microcephaly [MESH:D008831] (700)  Neuronal Migration Disorders [MESH:D054081] (264)  Tuberous Sclerosis [MESH:D014402] (635)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Knobloch syndrome [MESH:C537209] (70)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Peripheral Nervous System Neoplasms [MESH:D010524] (287)   Nerve Sheath Neoplasms [MESH:D018317] (286)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Tuberous Sclerosis [MESH:D014402] (635)  von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Canavan Disease [MESH:D017825] (29)  Huntington Disease [MESH:D006816] (540)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Tuberous Sclerosis [MESH:D014402] (635)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Prion Diseases [MESH:D017096] (475)   Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Neurologic Manifestations [MESH:D009461] (8964)   Gait Disorders, Neurologic [MESH:D020233] (491)  Neurogenic Inflammation [MESH:D020078] (2246)  Reflex, Abnormal [MESH:D012021] (485)  Urinary Bladder, Neurogenic [MESH:D001750] (113)  Dyskinesias [MESH:D020820] (3365)   Ataxia [MESH:D001259] (1138)  Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Tremor [MESH:D014202] (840)  Chorea [MESH:D002819] (189)   Paroxysmal nonkinesigenic dyskinesia [MESH:C537181] (23)  Generalized Epilepsy and Paroxysmal Dyskinesia [MESH:C563719] (51)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Nicolaides Baraitser syndrome [MESH:C536116] (40)  Coffin-Siris syndrome [MESH:C536436] (102)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Brunner Syndrome [MESH:C563156] (124)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Down Syndrome [MESH:D004314] (1287)  Williams Syndrome [MESH:D018980] (133)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Snyder Robinson syndrome [MESH:C536678] (19)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Psychomotor Disorders [MESH:D011596] (576)   Hypomyelination, Global Cerebral [MESH:C567847] (26)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Spasticity [MESH:D009128] (187)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Seizures [MESH:D012640] (4514)   Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency [MESH:C566449] (24)  Sensation Disorders [MESH:D012678] (5011)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 31 [MESH:C564629] (13)  Deafness, Autosomal Dominant 20 [MESH:C565754] (69)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Diseases [MESH:D009135] (3538)   VLCAD deficiency [MESH:C536353] (55)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency [MESH:C567709] (41)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 3 [MESH:C538350] (70)  Nemaline myopathy 4 [MESH:C538351] (47)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Myotonic Disorders [MESH:D020967] (138)   Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Mononeuropathies [MESH:D020422] (604)   Sciatic Neuropathy [MESH:D020426] (477)  Peripheral Nervous System Neoplasms [MESH:D010524] (287)   Nerve Sheath Neoplasms [MESH:D018317] (286)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)  Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)  Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Obstructive [MESH:D020181] (126)  Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Parasomnias [MESH:D020447] (453)   Sleep Arousal Disorders [MESH:D020921] (80)   Somnambulism [MESH:D013009] (75)   Epilepsy, Nocturnal Frontal Lobe, Type 4 [MESH:C563679] (43)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eyelid Diseases [MESH:D005141] (882)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Corneal Opacity [MESH:D003318] (544)   Peters anomaly [MESH:C537884] (465)  Eye Abnormalities [MESH:D005124] (1233)   Anterior segment mesenchymal dysgenesis [MESH:C537775] (20)  Peters anomaly [MESH:C537884] (465)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Coloboma [MESH:D003103] (315)   Papillorenal syndrome [MESH:C537168] (16)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Graves Ophthalmopathy [MESH:D049970] (165)  Eye Neoplasms [MESH:D005134] (413)   Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Cataract, posterior polar, 4 [MESH:C535344] (14)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma 3, Primary Congenital, A [MESH:C565547] (434)  Glaucoma, Open-Angle [MESH:D005902] (1281)   Glaucoma, Primary Open Angle [MESH:C562750] (466)  Glaucoma 1, Open Angle, A [MESH:C564234] (446)  Ocular Motility Disorders [MESH:D015835] (1699)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Refractive Errors [MESH:D012030] (457)   Myopia [MESH:D009216] (349)  Retinal Diseases [MESH:D012164] (3747)   Fundus Albipunctatus [MESH:C562733] (47)  Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinopathy of Prematurity [MESH:D012178] (353)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Juvenile macular degeneration and hypotrichosis [MESH:C537698] (34)  Macular Degeneration, Age-Related, 11 [MESH:C567450] (61)  Macular Edema [MESH:D008269] (557)  Retinal Detachment [MESH:D012163] (1639)   Knobloch syndrome [MESH:C537209] (70)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Aromatase deficiency [MESH:C537436] (277)  Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)   Follicle-stimulating hormone deficiency, isolated [MESH:C537070] (185)  Penile Diseases [MESH:D010409] (1805)   Penile Induration [MESH:D010411] (495)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Hyperplasia [MESH:D011470] (336)  Prostatic Neoplasms [MESH:D011471] (6135)  Prostatitis [MESH:D011472] (424)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)  Urogenital Abnormalities [MESH:D014564] (2065)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Cryptorchidism [MESH:D003456] (215)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Leydig Cell Hypoplasia [MESH:C562567] (65)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   46, XY Sex Reversal 5 [MESH:C567766] (19)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Dosage-sensitive sex reversal [MESH:C535601] (40)  Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)  Sexual Infantilism [MESH:D050035] (277)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   46, XY Sex Reversal 5 [MESH:C567766] (19)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Renal [MESH:D006977] (698)  Kidney Papillary Necrosis [MESH:D007681] (46)  Nephrocalcinosis [MESH:D009397] (311)  Zellweger Syndrome [MESH:D015211] (182)  Diabetes Insipidus [MESH:D003919] (354)   Diabetes Insipidus, Nephrogenic [MESH:D018500] (90)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Papillorenal syndrome [MESH:C537168] (16)  Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Renal hypouricemia [MESH:C537757] (71)  Hypouricemia, Renal, 2 [MESH:C567426] (32)  Bartter Syndrome [MESH:D001477] (241)  Fanconi Syndrome [MESH:D005198] (253)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Neurogenic [MESH:D001750] (113)  Urinary Bladder, Overactive [MESH:D053201] (530)  Vesico-Ureteral Reflux [MESH:D014718] (58)   Papillorenal syndrome [MESH:C537168] (16)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Oliguria [MESH:D009846] (307)  Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Sexual Dysfunction, Physiological [MESH:D012735] (270)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Anovulation [MESH:D000858] (59)  Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Primary Ovarian Insufficiency [MESH:D016649] (270)   Premature Ovarian Failure 7 [MESH:C567838] (52)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Uterine Diseases [MESH:D014591] (2479)   Uterine Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urogenital Abnormalities [MESH:D014564] (2043)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Leydig Cell Hypoplasia [MESH:C562567] (65)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   46, XY Sex Reversal 5 [MESH:C567766] (19)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Dosage-sensitive sex reversal [MESH:C535601] (40)  Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)  Sexual Infantilism [MESH:D050035] (277)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   46, XY Sex Reversal 5 [MESH:C567766] (19)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Renal [MESH:D006977] (698)  Kidney Papillary Necrosis [MESH:D007681] (46)  Nephrocalcinosis [MESH:D009397] (311)  Zellweger Syndrome [MESH:D015211] (182)  Diabetes Insipidus [MESH:D003919] (354)   Diabetes Insipidus, Nephrogenic [MESH:D018500] (90)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Papillorenal syndrome [MESH:C537168] (16)  Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Renal hypouricemia [MESH:C537757] (71)  Hypouricemia, Renal, 2 [MESH:C567426] (32)  Bartter Syndrome [MESH:D001477] (241)  Fanconi Syndrome [MESH:D005198] (253)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Neurogenic [MESH:D001750] (113)  Urinary Bladder, Overactive [MESH:D053201] (530)  Vesico-Ureteral Reflux [MESH:D014718] (58)   Papillorenal syndrome [MESH:C537168] (16)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Oliguria [MESH:D009846] (307)  Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71)  Pregnancy Complications [MESH:D011248] (4768)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Placenta Diseases [MESH:D010922] (1781)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870)  Puerperal Disorders [MESH:D011644] (324)   Lactation Disorders [MESH:D007775] (235)   Galactorrhea [MESH:D005687] (233) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Short QT Syndrome 3 [MESH:C566504] (39)  Short QT Syndrome 2 [MESH:C566505] (45)  Alagille Syndrome [MESH:D016738] (105)  Barth Syndrome [MESH:D056889] (13)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  Marfan Syndrome [MESH:D008382] (646)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 [MESH:C563409] (51)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)  Heart Diseases [MESH:D006331] (8614)   Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Short QT Syndrome 3 [MESH:C566504] (39)  Short QT Syndrome 2 [MESH:C566505] (45)  Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial Fibrillation, Familial, 3 [MESH:C563817] (60)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 3 [MESH:C567509] (44)  Brugada Syndrome 5 [MESH:C567556] (37)  Brugada Syndrome 7 [MESH:C567734] (31)  Heart Block [MESH:D006327] (571)   Sick Sinus Syndrome [MESH:D012804] (293)  Long QT Syndrome [MESH:D008133] (693)   Timothy syndrome [MESH:C536962] (44)  Long Qt Syndrome 5 [MESH:C566766] (40)  Andersen Syndrome [MESH:D050030] (39)  Jervell-Lange Nielsen Syndrome [MESH:D029593] (64)  Romano-Ward Syndrome [MESH:D029597] (47)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Polymorphic catecholergic ventricular tachycardia [MESH:C536334] (64)  Torsades de Pointes [MESH:D016171] (880)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1p [MESH:C563690] (45)  Cardiomyopathy, Dilated, 1M [MESH:C564390] (53)  Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)  Cardiomyopathy, Dilated, 1w [MESH:C566954] (66)  Cardiomyopathy, Dilated, 1AA [MESH:C567407] (27)  Cardiomyopathy, Dilated, 1z [MESH:C567506] (41)  Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathy, Dilated, 1EE [MESH:C567683] (61)  Cardiomyopathy, Dilated, 1BB [MESH:C567877] (31)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Endomyocardial Fibrosis [MESH:D004719] (521)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 [MESH:C563409] (51)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1p [MESH:C563690] (45)  Cardiomyopathy, Dilated, 1M [MESH:C564390] (53)  Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)  Cardiomyopathy, Dilated, 1w [MESH:C566954] (66)  Cardiomyopathy, Dilated, 1AA [MESH:C567407] (27)  Cardiomyopathy, Dilated, 1z [MESH:C567506] (41)  Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathy, Dilated, 1EE [MESH:C567683] (61)  Cardiomyopathy, Dilated, 1BB [MESH:C567877] (31)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 10 [MESH:C563865] (42)  Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Cardiomyopathy, Familial Hypertrophic, 15 [MESH:C567681] (66)  Cardiomyopathy, Familial Hypertrophic, 14 [MESH:C567684] (61)  Cardiomyopathy, Familial Hypertrophic, 13 [MESH:C567686] (41)  Heart Defects, Congenital [MESH:D006330] (2443)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Short QT Syndrome 3 [MESH:C566504] (39)  Short QT Syndrome 2 [MESH:C566505] (45)  Barth Syndrome [MESH:D056889] (13)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  Marfan Syndrome [MESH:D008382] (646)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 [MESH:C563409] (51)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Aortic Stenosis, Supravalvular [MESH:D021921] (135)   Williams Syndrome [MESH:D018980] (133)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Supravalvular [MESH:D021921] (50)  Vascular Diseases [MESH:D014652] (8691)   Arteritis [MESH:D001167] (1084)  Hyperemia [MESH:D006940] (2372)  Retinal Vein Occlusion [MESH:D012170] (607)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Coronary Aneurysm [MESH:D003323] (204)  Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)  Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Coronary Artery Disease [MESH:D003324] (2685)  Atherosclerosis [MESH:D050197] (4188)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Hypoxia-Ischemia, Brain [MESH:D020925] (33)   Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency [MESH:C566449] (24)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Thromboembolism [MESH:D013923] (732)  Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thrombosis [MESH:D013927] (3101)   Thromboembolism [MESH:D013923] (732)  Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Malignant [MESH:D006974] (621)  Hypertension, Pregnancy-Induced [MESH:D046110] (397)  Hypertension, Renal [MESH:D006977] (698)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  No-Reflow Phenomenon [MESH:D054318] (277)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Raynaud Disease [MESH:D011928] (490)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084)  Behcet Syndrome [MESH:D001528] (1784)  Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Z. Exceptions (453)   Not Fully Specified [NFS] (453)  Hematologic Diseases [MESH:D006402] (6174)   Adenosine Triphosphate, Elevated, Of Erythrocytes [MESH:C566310] (78)  Methemoglobinemia [MESH:D008708] (850)  Pancytopenia [MESH:D010198] (332)  Polycythemia [MESH:D011086] (412)  Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Anemia, Hemolytic [MESH:D000743] (3083)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Heinz Body Anemias [MESH:C563030] (127)  Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)   Majeed syndrome [MESH:C537839] (33)  Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)  beta-Thalassemia [MESH:D017086] (458)  Hemoglobinuria, Paroxysmal [MESH:D006457] (293)   Bone Marrow failure syndromes [MESH:C536572] (248)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, hypochromic microcytic [MESH:C536357] (164)  Anemia, Iron-Deficiency [MESH:D018798] (547)  Anemia, Macrocytic [MESH:D000748] (382)   Anemia, Megaloblastic [MESH:D000749] (288)  Red-Cell Aplasia, Pure [MESH:D012010] (183)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Blood Coagulation Disorders [MESH:D001778] (1828)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Factor XI Deficiency [MESH:D005173] (33)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Coagulation Protein Disorders [MESH:D020147] (580)   Factor XI Deficiency [MESH:D005173] (33)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Kernicterus [MESH:D007647] (256)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Hemoglobinuria, Paroxysmal [MESH:D006457] (293)   Bone Marrow failure syndromes [MESH:C536572] (248)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Polycythemia Vera [MESH:D011087] (244)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)  beta-Thalassemia [MESH:D017086] (458)  Hemorrhagic Disorders [MESH:D006474] (3359)   Factor XI Deficiency [MESH:D005173] (33)  Thrombocythemia, Essential [MESH:D013920] (707)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Leukocyte Disorders [MESH:D007960] (2662)   Leukostasis [MESH:D018921] (769)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)  Lymphatic Diseases [MESH:D008206] (5167)   Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Thymus Neoplasms [MESH:D013953] (247)  Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Lymphedema [MESH:D008209] (162)   Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Splenic Diseases [MESH:D013158] (1323)   Hypersplenism [MESH:D006971] (341) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Drug-Induced [MESH:D000014] (1024)  Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Coffin-Siris syndrome [MESH:C536436] (102)  Van der Woude syndrome [MESH:C536528] (33)  Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  Pituitary Hormone Deficiency, Combined, 4 [MESH:C567492] (15)  Alagille Syndrome [MESH:D016738] (105)  Bardet-Biedl Syndrome [MESH:D020788] (110)  Barth Syndrome [MESH:D056889] (13)  Donohue Syndrome [MESH:D056731] (95)  Down Syndrome [MESH:D004314] (1287)  Incontinentia Pigmenti [MESH:D007184] (57)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Marfan Syndrome [MESH:D008382] (646)  Prolidase Deficiency [MESH:D056732] (46)  Zellweger Syndrome [MESH:D015211] (182)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Ectodermal Dysplasia [MESH:D004476] (938)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Waardenburg Syndrome [MESH:D014849] (243)   ABCD syndrome [MESH:C535334] (143)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Short QT Syndrome 3 [MESH:C566504] (39)  Short QT Syndrome 2 [MESH:C566505] (45)  Alagille Syndrome [MESH:D016738] (105)  Barth Syndrome [MESH:D056889] (13)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  Marfan Syndrome [MESH:D008382] (646)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 [MESH:C563409] (51)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)  Long QT Syndrome [MESH:D008133] (693)   Timothy syndrome [MESH:C536962] (44)  Long Qt Syndrome 5 [MESH:C566766] (40)  Andersen Syndrome [MESH:D050030] (39)  Jervell-Lange Nielsen Syndrome [MESH:D029593] (64)  Romano-Ward Syndrome [MESH:D029597] (47)  Chromosome Disorders [MESH:D025063] (2030)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Down Syndrome [MESH:D004314] (1287)  Williams Syndrome [MESH:D018980] (133)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)  Eye Abnormalities [MESH:D005124] (1233)   Anterior segment mesenchymal dysgenesis [MESH:C537775] (20)  Peters anomaly [MESH:C537884] (465)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Coloboma [MESH:D003103] (315)   Papillorenal syndrome [MESH:C537168] (16)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Hajdu-Cheney Syndrome [MESH:D031845] (42)  Arthrogryposis [MESH:D001176] (329)   Distal arthrogryposis type 2B [MESH:C538400] (85)  Craniofacial Abnormalities [MESH:D019465] (3064)   Frontonasal dysplasia [MESH:C538065] (52)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Cleidocranial Dysplasia [MESH:D002973] (129)  Craniosynostoses [MESH:D003398] (438)  Microcephaly [MESH:D008831] (700)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Split-Hand/Foot Malformation 6 [MESH:C567616] (29)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Brachydactyly [MESH:D059327] (220)  Foot Deformities, Congenital [MESH:D005532] (538)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Eiken Skeletal Dysplasia [MESH:C564010] (40)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Hand Deformities, Congenital [MESH:D006228] (587)   Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Coffin-Siris syndrome [MESH:C536436] (102)  Eiken Skeletal Dysplasia [MESH:C564010] (40)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Lower Extremity Deformities, Congenital [MESH:D038061] (81)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Nervous System Malformations [MESH:D009421] (3354)   Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)  Microcephaly [MESH:D008831] (700)  Neuronal Migration Disorders [MESH:D054081] (264)  Tuberous Sclerosis [MESH:D014402] (635)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Knobloch syndrome [MESH:C537209] (70)  Skin Abnormalities [MESH:D012868] (1723)   Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma [MESH:C566600] (15)  Incontinentia Pigmenti [MESH:D007184] (57)  Prolidase Deficiency [MESH:D056732] (46)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Acrodermatitis [MESH:D000169] (56)   Acrodermatitis enteropathica [MESH:C538178] (51)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Xeroderma Pigmentosum [MESH:D014983] (213)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Orofacial Cleft 11 [MESH:C567410] (101)  Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Orofacial Cleft 11 [MESH:C567410] (101)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anodontia [MESH:D000848] (185)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Hypomaturation Type, Iia3 [MESH:C567706] (12)  Urogenital Abnormalities [MESH:D014564] (2064)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microphthalmia, Syndromic 6 [MESH:C566440] (101)  Cryptorchidism [MESH:D003456] (215)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Leydig Cell Hypoplasia [MESH:C562567] (65)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   46, XY Sex Reversal 5 [MESH:C567766] (19)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Dosage-sensitive sex reversal [MESH:C535601] (40)  Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)  Sexual Infantilism [MESH:D050035] (277)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   46, XY Sex Reversal 5 [MESH:C567766] (19)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Alagille Syndrome [MESH:D016738] (105)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Cystic Fibrosis [MESH:D003550] (760)  Donohue Syndrome [MESH:D056731] (95)  Hajdu-Cheney Syndrome [MESH:D031845] (42)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Marfan Syndrome [MESH:D008382] (646)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Heinz Body Anemias [MESH:C563030] (127)  Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)   Majeed syndrome [MESH:C537839] (33)  Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)  beta-Thalassemia [MESH:D017086] (458)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Factor XI Deficiency [MESH:D005173] (33)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 3 [MESH:C567509] (44)  Brugada Syndrome 5 [MESH:C567556] (37)  Brugada Syndrome 7 [MESH:C567734] (31)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 10 [MESH:C563865] (42)  Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Cardiomyopathy, Familial Hypertrophic, 15 [MESH:C567681] (66)  Cardiomyopathy, Familial Hypertrophic, 14 [MESH:C567684] (61)  Cardiomyopathy, Familial Hypertrophic, 13 [MESH:C567686] (41)  Chromosome Disorders [MESH:D025063] (2030)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Down Syndrome [MESH:D004314] (1287)  Williams Syndrome [MESH:D018980] (133)  Dwarfism [MESH:D004392] (783)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Brunner Syndrome [MESH:C563156] (124)  Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Atypical Mycobacteriosis, Familial, X-Linked 1 [MESH:C567070] (56)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Barth Syndrome [MESH:D056889] (13)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Snyder Robinson syndrome [MESH:C536678] (19)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)  beta-Thalassemia [MESH:D017086] (458)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Canavan Disease [MESH:D017825] (29)  Huntington Disease [MESH:D006816] (540)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Tuberous Sclerosis [MESH:D014402] (635)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Snyder Robinson syndrome [MESH:C536678] (19)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Metabolism, Inborn Errors [MESH:D008661] (6032)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Aromatase deficiency [MESH:C537436] (277)  Xanthinuria, Type I [MESH:C562584] (190)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Porphyrias [MESH:D011164] (917)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Sulfite oxidase deficiency [MESH:C538141] (27)  3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency [MESH:C538324] (36)  Hyperprolinemia [MESH:C538384] (45)  Hyperprolinemia type 2 [MESH:C538385] (39)  Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  Methylmalonic Aciduria and Homocystinuria, CblD Type [MESH:C564743] (10)  Maple Syrup Urine Disease [MESH:D008375] (127)  Prolidase Deficiency [MESH:D056732] (46)  Tyrosinemias [MESH:D020176] (132)  Hyperhomocysteinemia [MESH:D020138] (1724)   Homocystinuria [MESH:D006712] (93)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Galactosemias [MESH:D005693] (69)  Homocystinuria [MESH:D006712] (93)  Leigh Disease [MESH:D007888] (206)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Maple Syrup Urine Disease [MESH:D008375] (127)  Tyrosinemias [MESH:D020176] (132)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Canavan Disease [MESH:D017825] (29)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Peroxisomal Disorders [MESH:D018901] (1472)   Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  De Vivo disease [MESH:C536830] (172)  Galactosemias [MESH:D005693] (69)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Congenital Disorder of Glycosylation, Type Io [MESH:C567857] (14)  Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease XII [MESH:C562718] (98)  Glycogen Storage Disease IC [MESH:C562805] (53)  Glycogen Storage Disease Type VI [MESH:D006013] (73)  Glycogen Storage Disease Type I [MESH:D005953] (140)   Glycogen Storage Disease IB [MESH:C562594] (53)  Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Leigh Disease [MESH:D007888] (206)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Gilbert Disease [MESH:D005878] (259)  Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Crigler-Najjar Syndrome [MESH:D003414] (255)   Crigler Najjar syndrome, type 2 [MESH:C536213] (254)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  VLCAD deficiency [MESH:C536353] (55)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Barth Syndrome [MESH:D056889] (13)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Hypolipoproteinemias [MESH:D007009] (365)   Hypobetalipoproteinemias [MESH:D006995] (88)   Abetalipoproteinemia [MESH:D000012] (63)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hypophosphatasia [MESH:D007014] (142)   Hypophosphatasia, Childhood [MESH:C562440] (137)  Hypophosphatasia, Infantile [MESH:C562646] (137)  Hypophosphatasia, Adult [MESH:C562647] (137)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Gout [MESH:D006073] (261)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Renal hypouricemia [MESH:C537757] (71)  Hypouricemia, Renal, 2 [MESH:C567426] (32)  Fanconi Syndrome [MESH:D005198] (253)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Lathosterolosis [MESH:C537880] (66)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Mineralocorticoid Excess Syndrome, Apparent [MESH:D043204] (121)   Apparent mineralocorticoid excess [MESH:C537422] (120)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency [MESH:C567709] (41)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Tuberous Sclerosis [MESH:D014402] (635)  Wilms Tumor [MESH:D009396] (553)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Skin Diseases, Genetic [MESH:D012873] (3456)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma [MESH:C566600] (15)  Cutis Laxa [MESH:D003483] (177)  Darier Disease [MESH:D007644] (125)  Dermatitis, Atopic [MESH:D003876] (2052)  Incontinentia Pigmenti [MESH:D007184] (57)  Prolidase Deficiency [MESH:D056732] (46)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Papillon-Lefevre Disease [MESH:D010214] (76)   Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Xeroderma Pigmentosum [MESH:D014983] (213)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal [MESH:C563463] (52)  Asphyxia Neonatorum [MESH:D001238] (1648)  Congenital Hyperinsulinism [MESH:D044903] (132)  Cystic Fibrosis [MESH:D003550] (760)  Erythroblastosis, Fetal [MESH:D004899] (257)   Kernicterus [MESH:D007647] (256)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Jaundice, Neonatal [MESH:D007567] (290)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Ichthyosis [MESH:D007057] (476)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Infant, Premature, Diseases [MESH:D007235] (1292)   Retinopathy of Prematurity [MESH:D012178] (353)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Cartilage Diseases [MESH:D002357] (438)  Cutis Laxa [MESH:D003483] (177)  Dermatomyositis [MESH:D003882] (1826)  Homocystinuria [MESH:D006712] (93)  Marfan Syndrome [MESH:D008382] (646)  Penile Induration [MESH:D010411] (495)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Dermatomyositis [MESH:D003882] (1826)  Erythema [MESH:D004890] (1330)  Pruritus [MESH:D011537] (647)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Skin Neoplasms [MESH:D012878] (2991)  Skin Ulcer [MESH:D012883] (229)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Gynecomastia [MESH:D006177] (484)   Aromatase deficiency [MESH:C537436] (277)  Lactation Disorders [MESH:D007775] (235)   Galactorrhea [MESH:D005687] (233)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Drug Eruptions [MESH:D003875] (2697)  Acrodermatitis [MESH:D000169] (56)   Acrodermatitis enteropathica [MESH:C538178] (51)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136)  Hypotrichosis [MESH:D007039] (1513)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Juvenile macular degeneration and hypotrichosis [MESH:C537698] (34)  Alopecia [MESH:D000505] (1453)  Keratosis [MESH:D007642] (1941)   Darier Disease [MESH:D007644] (125)  Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Papillon-Lefevre Disease [MESH:D010214] (76)   Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Photosensitivity Disorders [MESH:D010787] (272)   Xeroderma Pigmentosum [MESH:D014983] (213)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Pigmentation Disorders [MESH:D010859] (1215)   Cafe-au-Lait Spots [MESH:D019080] (186)  Incontinentia Pigmenti [MESH:D007184] (57)  Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Acanthosis Nigricans [MESH:D000052] (203)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Xeroderma Pigmentosum [MESH:D014983] (213)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Skin Abnormalities [MESH:D012868] (1709)   Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma [MESH:C566600] (15)  Incontinentia Pigmenti [MESH:D007184] (57)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Acrodermatitis [MESH:D000169] (56)   Acrodermatitis enteropathica [MESH:C538178] (51)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Xeroderma Pigmentosum [MESH:D014983] (213)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma [MESH:C566600] (15)  Cutis Laxa [MESH:D003483] (177)  Darier Disease [MESH:D007644] (125)  Dermatitis, Atopic [MESH:D003876] (2052)  Incontinentia Pigmenti [MESH:D007184] (57)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)  Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Papillon-Lefevre Disease [MESH:D010214] (76)   Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Xeroderma Pigmentosum [MESH:D014983] (213)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Z. Exceptions (817)   Not Fully Specified [NFS] (817)  Metabolic Diseases [MESH:D008659] (9025)   Porphyrias [MESH:D011164] (917)  Acid-Base Imbalance [MESH:D000137] (854)   Alkalosis [MESH:D000471] (384)  Acidosis [MESH:D000138] (626)   Ketosis [MESH:D007662] (234)   Diabetic Ketoacidosis [MESH:D016883] (226)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency [MESH:C566449] (24)  Hepatic Encephalopathy [MESH:D006501] (1795)  Kernicterus [MESH:D007647] (256)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Galactosemias [MESH:D005693] (69)  Homocystinuria [MESH:D006712] (93)  Leigh Disease [MESH:D007888] (206)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Maple Syrup Urine Disease [MESH:D008375] (127)  Tyrosinemias [MESH:D020176] (132)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Canavan Disease [MESH:D017825] (29)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Peroxisomal Disorders [MESH:D018901] (1472)   Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  Nephrocalcinosis [MESH:D009397] (311)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Fanconi Anemia [MESH:D005199] (1604)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  Xeroderma Pigmentosum [MESH:D014983] (213)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetic Ketoacidosis [MESH:D016883] (226)  Donohue Syndrome [MESH:D056731] (95)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225)  Diabetes Mellitus, Insulin-Dependent, 20 [MESH:C567286] (49)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 3 [MESH:C563933] (49)  Maturity-Onset Diabetes of the Young, Type 2 [MESH:C564219] (82)  Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic hypoglycemia, familial, 3 [MESH:C538374] (82)  Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Hyperinsulinemic Hypoglycemia, Familial, 5 [MESH:C566494] (94)  Congenital Hyperinsulinism [MESH:D044903] (132)  Insulin Resistance [MESH:D007333] (3511)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Hypoglycemia [MESH:D007003] (2420)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Hyperinsulinemic hypoglycemia, familial, 3 [MESH:C538374] (82)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Hyperinsulinemic Hypoglycemia, Familial, 5 [MESH:C566494] (94)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Congenital Hyperinsulinism [MESH:D044903] (132)  Iron Metabolism Disorders [MESH:D019189] (2139)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Hypertriglyceridemia [MESH:D015228] (808)   Hyperlipoproteinemia Type V [MESH:D006954] (37)  Hypolipoproteinemias [MESH:D007009] (409)   Hypobetalipoproteinemias [MESH:D006995] (181)   Abetalipoproteinemia [MESH:D000012] (63)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  VLCAD deficiency [MESH:C536353] (55)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Metabolism, Inborn Errors [MESH:D008661] (6028)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Aromatase deficiency [MESH:C537436] (277)  Xanthinuria, Type I [MESH:C562584] (190)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Porphyrias [MESH:D011164] (917)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Sulfite oxidase deficiency [MESH:C538141] (27)  3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency [MESH:C538324] (36)  Hyperprolinemia [MESH:C538384] (45)  Hyperprolinemia type 2 [MESH:C538385] (39)  Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  Methylmalonic Aciduria and Homocystinuria, CblD Type [MESH:C564743] (10)  Maple Syrup Urine Disease [MESH:D008375] (127)  Tyrosinemias [MESH:D020176] (132)  Hyperhomocysteinemia [MESH:D020138] (1724)   Homocystinuria [MESH:D006712] (93)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Galactosemias [MESH:D005693] (69)  Homocystinuria [MESH:D006712] (93)  Leigh Disease [MESH:D007888] (206)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Maple Syrup Urine Disease [MESH:D008375] (127)  Tyrosinemias [MESH:D020176] (132)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Canavan Disease [MESH:D017825] (29)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Peroxisomal Disorders [MESH:D018901] (1472)   Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  De Vivo disease [MESH:C536830] (172)  Galactosemias [MESH:D005693] (69)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Congenital Disorder of Glycosylation, Type Io [MESH:C567857] (14)  Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease XII [MESH:C562718] (98)  Glycogen Storage Disease IC [MESH:C562805] (53)  Glycogen Storage Disease Type VI [MESH:D006013] (73)  Glycogen Storage Disease Type I [MESH:D005953] (140)   Glycogen Storage Disease IB [MESH:C562594] (53)  Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Leigh Disease [MESH:D007888] (206)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Gilbert Disease [MESH:D005878] (259)  Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Crigler-Najjar Syndrome [MESH:D003414] (255)   Crigler Najjar syndrome, type 2 [MESH:C536213] (254)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  VLCAD deficiency [MESH:C536353] (55)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Neutral Lipid Storage Disease with Myopathy [MESH:C565192] (58)  Barth Syndrome [MESH:D056889] (13)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Hypolipoproteinemias [MESH:D007009] (365)   Hypobetalipoproteinemias [MESH:D006995] (88)   Abetalipoproteinemia [MESH:D000012] (63)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Tay-Sachs Disease [MESH:D013661] (34)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)   Niemann-Pick disease, type C2 [MESH:C536119] (43)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hypophosphatasia [MESH:D007014] (142)   Hypophosphatasia, Childhood [MESH:C562440] (137)  Hypophosphatasia, Infantile [MESH:C562646] (137)  Hypophosphatasia, Adult [MESH:C562647] (137)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Gout [MESH:D006073] (261)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Renal hypouricemia [MESH:C537757] (71)  Hypouricemia, Renal, 2 [MESH:C567426] (32)  Fanconi Syndrome [MESH:D005198] (253)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Lathosterolosis [MESH:C537880] (66)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Mineralocorticoid Excess Syndrome, Apparent [MESH:D043204] (121)   Apparent mineralocorticoid excess [MESH:C537422] (120)  Mitochondrial Diseases [MESH:D028361] (2561)   VLCAD deficiency [MESH:C536353] (55)  Mitochondrial complex I deficiency [MESH:C537475] (140)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal [MESH:C563463] (52)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Hypomyelination, Global Cerebral [MESH:C567847] (26)  Leigh Disease [MESH:D007888] (206)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hyperkalemia [MESH:D006947] (485)  Hypokalemia [MESH:D007008] (1041)  Hyponatremia [MESH:D007010] (789)  Inappropriate ADH Syndrome [MESH:D007177] (178)   Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)  Vitamin B Deficiency [MESH:D014804] (1817)   Folic Acid Deficiency [MESH:D005494] (134)  Hyperhomocysteinemia [MESH:D020138] (1716)  Vitamin D Deficiency [MESH:D014808] (360)   Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Obesity, Abdominal [MESH:D056128] (115)  Obesity, Morbid [MESH:D009767] (515)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Z. Exceptions (123)   Not Fully Specified [NFS] (123)  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Hyperaldosteronism [MESH:D006929] (419)   Bartter Syndrome [MESH:D001477] (241)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Donohue Syndrome [MESH:D056731] (95)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Ketoacidosis [MESH:D016883] (226)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225)  Diabetes Mellitus, Insulin-Dependent, 20 [MESH:C567286] (49)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 3 [MESH:C563933] (49)  Maturity-Onset Diabetes of the Young, Type 2 [MESH:C564219] (82)  Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)  Dwarfism [MESH:D004392] (698)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 4 [MESH:C567492] (15)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroid cancer, Hurthle cell [MESH:C536913] (24)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Delayed [MESH:D011628] (449)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Leydig Cell Hypoplasia [MESH:C562567] (65)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   46, XY Sex Reversal 5 [MESH:C567766] (19)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Dosage-sensitive sex reversal [MESH:C535601] (40)  Gonadal Dysgenesis, 46,XX [MESH:D023961] (56)  Sexual Infantilism [MESH:D050035] (277)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   46, XY Sex Reversal 5 [MESH:C567766] (19)  Hypogonadism [MESH:D007006] (1123)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Sexual Infantilism [MESH:D050035] (277)  Ovarian Diseases [MESH:D010049] (4253)   Anovulation [MESH:D000858] (59)  Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Primary Ovarian Insufficiency [MESH:D016649] (270)   Premature Ovarian Failure 7 [MESH:C567838] (52)  Puberty, Precocious [MESH:D011629] (1147)   Familial Testotoxicosis [MESH:C536961] (65)  Testicular Diseases [MESH:D013733] (777)   Cryptorchidism [MESH:D003456] (215)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)  Pituitary Diseases [MESH:D010900] (1829)   Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Hyperprolactinemia [MESH:D006966] (603)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Gigantism [MESH:D005877] (46)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Hypopituitarism [MESH:D007018] (732)   Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 4 [MESH:C567492] (15)  Inappropriate ADH Syndrome [MESH:D007177] (178)   Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroidism [MESH:D006980] (1191)   Thyroid Hormone Resistance, Selective Pituitary [MESH:C564154] (113)  Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroxinemia [MESH:D006981] (659)   Thyroid Hormone Resistance Syndrome [MESH:D018382] (135)   Thyroid Hormone Resistance, Generalized, Autosomal Dominant [MESH:C567934] (113)  Thyroid Hormone Resistance, Generalized, Autosomal Recessive [MESH:C567936] (113)  Hypothyroidism [MESH:D007037] (496)   Thyroid Dyshormonogenesis 3 [MESH:C562769] (46)  Pituitary Hormone Deficiency, Combined, 4 [MESH:C567492] (15)  Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroid cancer, Hurthle cell [MESH:C536913] (24)  Thyroiditis [MESH:D013966] (158)   Thyroiditis, Autoimmune [MESH:D013967] (149)   Hashimoto Disease [MESH:D050031] (98) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Thyroiditis, Autoimmune [MESH:D013967] (79)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)   Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225)  Diabetes Mellitus, Insulin-Dependent, 20 [MESH:C567286] (49)  Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Kernicterus [MESH:D007647] (256)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)  Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Food Hypersensitivity [MESH:D005512] (608)   Peanut Hypersensitivity [MESH:D021183] (572)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (3914)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Immunodeficiency without anhidrotic ectodermal dysplasia [MESH:C536289] (56)  Invasive Pneumococcal Disease, Recurrent Isolated, 2 [MESH:C564468] (56)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Complement Component 6 Deficiency [MESH:C567307] (35)  HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Hepatitis, Animal [MESH:D006520] (260)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Salmonella Infections, Animal [MESH:D012481] (604)  Cattle Diseases [MESH:D002418] (416)   Tuberculosis, Bovine [MESH:D014380] (380)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Plaque, Atherosclerotic [MESH:D058226] (696)  Ventricular Remodeling [MESH:D020257] (686)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Gallstones [MESH:D042882] (350)  Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71)  Cysts [MESH:D003560] (133)   Van der Woude syndrome [MESH:C536528] (33)  Hernia [MESH:D006547] (2825)   Encephalocele [MESH:D004677] (151)   Knobloch syndrome [MESH:C537209] (70)  Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Hypertrophy [MESH:D006984] (4476)   Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)   Colonic Polyps [MESH:D003111] (210)  Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Pathologic Processes [MESH:D010335] (9863)   Azotemia [MESH:D053099] (326)  Emphysema [MESH:D004646] (1096)  Gliosis [MESH:D005911] (1419)  Hyperplasia [MESH:D006965] (2463)  Hyperuricemia [MESH:D033461] (82)  Lithiasis [MESH:D020347] (345)  Muscle Weakness [MESH:D018908] (478)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Short QT Syndrome 3 [MESH:C566504] (39)  Short QT Syndrome 2 [MESH:C566505] (45)  Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial Fibrillation, Familial, 3 [MESH:C563817] (60)  Heart Block [MESH:D006327] (571)   Sick Sinus Syndrome [MESH:D012804] (293)  Long QT Syndrome [MESH:D008133] (691)   Timothy syndrome [MESH:C536962] (44)  Long Qt Syndrome 5 [MESH:C566766] (40)  Andersen Syndrome [MESH:D050030] (39)  Romano-Ward Syndrome [MESH:D029597] (47)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Polymorphic catecholergic ventricular tachycardia [MESH:C536334] (64)  Torsades de Pointes [MESH:D016171] (880)  Chromosome Aberrations [MESH:D002869] (2352)   Chromosomal Instability [MESH:D043171] (67)  Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Translocation, Genetic [MESH:D014178] (557)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)   Sudden Infant Death [MESH:D013398] (268)  Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Disease Attributes [MESH:D020969] (3654)   Critical Illness [MESH:D016638] (296)  Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Facies [MESH:D019066] (738)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Fibrosis [MESH:D005355] (3133)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Genomic Instability [MESH:D042822] (184)   Chromosomal Instability [MESH:D043171] (67)  Granuloma [MESH:D006099] (587)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Growth Disorders [MESH:D006130] (2438)   Meier-Gorlin syndrome [MESH:C538012] (133)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Spondyloepimetaphyseal Dysplasia, Pakistani Type [MESH:C567551] (63)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Hyperbilirubinemia [MESH:D006932] (1860)   Kernicterus [MESH:D007647] (256)  Hyperbilirubinemia, Neonatal [MESH:D051556] (258)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Ischemia [MESH:D007511] (3049)   Infarction [MESH:D007238] (298)  No-Reflow Phenomenon [MESH:D054318] (277)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Necrosis [MESH:D009336] (4019)   Infarction [MESH:D007238] (298)  Osteonecrosis [MESH:D010020] (537)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Ossification, Heterotopic [MESH:D009999] (187)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Postoperative Complications [MESH:D011183] (5311)   Pain, Postoperative [MESH:D010149] (529)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Chills [MESH:D023341] (644)  Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Feminization [MESH:D005262] (655)  Reticulocytosis [MESH:D045262] (514)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)   Obesity, Morbid [MESH:D009767] (515)  Neurologic Manifestations [MESH:D009461] (8702)   Gait Disorders, Neurologic [MESH:D020233] (491)  Reflex, Abnormal [MESH:D012021] (485)  Urinary Bladder, Neurogenic [MESH:D001750] (113)  Dyskinesias [MESH:D020820] (3285)   Ataxia [MESH:D001259] (984)  Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Tremor [MESH:D014202] (840)  Chorea [MESH:D002819] (189)   Paroxysmal nonkinesigenic dyskinesia [MESH:C537181] (23)  Generalized Epilepsy and Paroxysmal Dyskinesia [MESH:C563719] (51)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Nicolaides Baraitser syndrome [MESH:C536116] (40)  Coffin-Siris syndrome [MESH:C536436] (102)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Brunner Syndrome [MESH:C563156] (124)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Psychomotor Disorders [MESH:D011596] (576)   Hypomyelination, Global Cerebral [MESH:C567847] (26)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Spasticity [MESH:D009128] (187)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Seizures [MESH:D012640] (4502)   Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency [MESH:C566449] (24)  Sensation Disorders [MESH:D012678] (5009)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 31 [MESH:C564629] (13)  Deafness, Autosomal Dominant 20 [MESH:C565754] (69)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Pain, Postoperative [MESH:D010149] (529)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Hyperphagia [MESH:D006963] (206)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperoxia [MESH:D018496] (694)  Hyperventilation [MESH:D006985] (652)  Respiratory Sounds [MESH:D012135] (713)  Hypoventilation [MESH:D007040] (359)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Skin Manifestations [MESH:D012877] (1250)   Cafe-au-Lait Spots [MESH:D019080] (186)  Pruritus [MESH:D011537] (648)  Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Urological Manifestations [MESH:D020924] (3532)   Oliguria [MESH:D009846] (307)  Lower Urinary Tract Symptoms [MESH:D059411] (612)   Urinary Bladder, Overactive [MESH:D053201] (530)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Virilism [MESH:D014770] (327)   Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)  Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Foodborne Diseases [MESH:D005517] (269)  Lead Poisoning [MESH:D007855] (515)  Manganese Poisoning [MESH:D020149] (2214)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Drug Overdose [MESH:D062787] (513)  Marijuana Abuse [MESH:D002189] (1132)  Phencyclidine Abuse [MESH:D010623] (288)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950)  Morphine Dependence [MESH:D009021] (855) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Fractures, Bone [MESH:D050723] (597)  Heat Stress Disorders [MESH:D018882] (226)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Neoplasms, Radiation-Induced [MESH:D009381] (171)  Radiation Injuries, Experimental [MESH:D011833] (2662)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Carboxylic Acids [MESH:D002264] (13103)   Acids, Carbocyclic [MESH:D000146] (5074)   Phthalic Acids [MESH:D010795] (403)   Diethylhexyl Phthalate [MESH:D004051] (4) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Diagnostic Imaging [MESH:D003952] (623)   Ultrasonography [MESH:D014463] (482)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Diagnostic Techniques, Cardiovascular [MESH:D003935] (521)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Physical Examination [MESH:D010808] (1041)   Facies [MESH:D019066] (704)   Nicolaides Baraitser syndrome [MESH:C536116] (40)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Behavior [MESH:D001519] (335)   Behavioral Symptoms [MESH:D001526] (173)   Aggression [MESH:D000374] (127)   Brunner Syndrome [MESH:C563156] (124)  Social Behavior [MESH:D012919] (163)   Aggression [MESH:D000374] (125)   Brunner Syndrome [MESH:C563156] (124)  Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Nicolaides Baraitser syndrome [MESH:C536116] (40)  Coffin-Siris syndrome [MESH:C536436] (102)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Brunner Syndrome [MESH:C563156] (124)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Psychomotor Disorders [MESH:D011596] (250)   Hypomyelination, Global Cerebral [MESH:C567847] (26)  Mental Disorders [MESH:D001523] (2063)   Impulse Control Disorders [MESH:D007174] (128)   Brunner Syndrome [MESH:C563156] (124)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   De Sanctis-Cacchione syndrome [MESH:C535992] (27)  Nicolaides Baraitser syndrome [MESH:C536116] (40)  Coffin-Siris syndrome [MESH:C536436] (102)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Brunner Syndrome [MESH:C563156] (124)  Cerebral Cavernous Malformations 3 [MESH:C566393] (27)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XX Disorders of Sex Development [MESH:D058489] (375)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (388)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Leydig Cell Hypoplasia [MESH:C562567] (65)  Sleep Disorders [MESH:D012893] (148)   Parasomnias [MESH:D020447] (57)   Sleep Arousal Disorders [MESH:D020921] (46)   Somnambulism [MESH:D013009] (44)   Epilepsy, Nocturnal Frontal Lobe, Type 4 [MESH:C563679] (43) G. Phenomena and Processes  G. Phenomena and Processes  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 21-22 and Y [MESH:D002904] (294)   Chromosomes, Human, Pair 22 [MESH:D002892] (250)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Physiological Phenomena [MESH:D010829] (788)   Pharmacological Phenomena [MESH:D002620] (173)   Drug Resistance [MESH:D004351] (139)   Insulin Resistance [MESH:D007333] (97)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Circulatory and Respiratory Physiological Phenomena [MESH:D002943] (614)   Cardiovascular Physiological Phenomena [MESH:D002320] (525)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)