Item 26 of 82 (back to results) previous next   Chloroprene D002737               MeSH Unique Identifier: D002737 Scope Notes: Toxic, possibly carcinogenic, monomer of neoprene, a synthetic rubber; causes damage to skin, lungs, CNS, kidneys, liver, blood cells and fetuses. Synonym: 2-chlorobutadiene. 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 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)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Face [MESH:D005145] (387)   Coffin-Siris syndrome [MESH:C536436] (102)  Eye [MESH:D005123] (148)   Eyelids [MESH:D005143] (143)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  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)   Muscles [MESH:D009132] (97)   Muscle, Skeletal [MESH:D018482] (86)   Abdominal Muscles [MESH:D000009] (49)   Carnevale syndrome [MESH:C535586] (45)  Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Foot Bones [MESH:D005529] (51)   Tarsal Bones [MESH:D013639] (43)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Pelvic Bones [MESH:D010384] (41)   Al Awadi syndrome [MESH:C535612] (30)  Bones of Upper Extremity [MESH:D001133] (240)   Arm Bones [MESH:D050280] (183)   Radius [MESH:D011884] (126)   VATER association [MESH:C536534] (46)  Hand Bones [MESH:D050276] (59)   Carpal Bones [MESH:D002348] (49)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  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)  Spine [MESH:D013131] (258)   VATER association [MESH:C536534] (46)  Sacrum [MESH:D012447] (50)   Currarino triad [MESH:C536221] (47)  Joints [MESH:D007596] (126)   Hand Joints [MESH:D050823] (57)   Finger Joint [MESH:D005384] (46)   Cushing's symphalangism [MESH:C536223] (42)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Intestines [MESH:D007422] (271)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   Currarino triad [MESH:C536221] (47)  Rectum [MESH:D012007] (69)   Currarino triad [MESH:C536221] (47)  Lower Gastrointestinal Tract [MESH:D041741] (254)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   Currarino triad [MESH:C536221] (47)  Rectum [MESH:D012007] (69)   Currarino triad [MESH:C536221] (47)  Upper Gastrointestinal Tract [MESH:D041742] (236)   Esophagus [MESH:D004947] (200)   VATER association [MESH:C536534] (46)  Respiratory System [MESH:D012137] (321)   Nose [MESH:D009666] (91)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Trachea [MESH:D014132] (190)   VATER association [MESH:C536534] (46)  Urogenital System [MESH:D014566] (986)   Genitalia [MESH:D005835] (400)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Genitalia, Female [MESH:D005836] (66)   Uterus [MESH:D014599] (43)   Al Awadi syndrome [MESH:C535612] (30)  Nervous System [MESH:D009420] (587)   Central Nervous System [MESH:D002490] (371)   Brain [MESH:D001921] (349)   Brain Stem [MESH:D001933] (120)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Ear, Middle [MESH:D004432] (49)   Ear Ossicles [MESH:D004429] (40)   Stapes [MESH:D013199] (36)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Peters anomaly [MESH:C537884] (465)  Eyelids [MESH:D005143] (146)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Nose [MESH:D009666] (74)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  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)   Dentition [MESH:D003817] (109)   Tooth [MESH:D014070] (61)   Incisor [MESH:D007180] (51)   Single upper central incisor [MESH:C537342] (50) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Bacteremia [MESH:D016470] (208)  Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Leprosy [MESH:D007918] (261)  Tuberculosis [MESH:D014376] (992)  Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)   Atypical Mycobacteriosis, Familial, X-Linked 1 [MESH:C567070] (56)  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)   Pyogenic arthritis, pyoderma gangrenosum, and acne [MESH:C536253] (15)  Bone Diseases, Infectious [MESH:D001850] (90)   Osteomyelitis [MESH:D010019] (69)   Majeed syndrome [MESH:C537839] (33)  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)  Skin Diseases, Infectious [MESH:D012874] (415)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)   Candidiasis familial chronic mucocutaneous, autosomal recessive [MESH:C537979] (36)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289)  Mycoses [MESH:D009181] (385)   Candidiasis [MESH:D002177] (307)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)   Candidiasis familial chronic mucocutaneous, autosomal recessive [MESH:C537979] (36)  Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)   Candidiasis familial chronic mucocutaneous, autosomal recessive [MESH:C537979] (36) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Arbovirus Infections [MESH:D001102] (150)   Encephalitis, Arbovirus [MESH:D004671] (78)   West Nile Fever [MESH:D014901] (73)  Central Nervous System Viral Diseases [MESH:D020805] (1416)   Encephalitis [MESH:D004660] (226)   Encephalitis, Viral [MESH:D018792] (183)   Encephalitis, Arbovirus [MESH:D004671] (78)   West Nile Fever [MESH:D014901] (73)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Herpesviridae Infections [MESH:D006566] (1944)   Cytomegalovirus Infections [MESH:D003586] (222)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Papillomavirus Infections [MESH:D030361] (630)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Encephalitis, Viral [MESH:D018792] (183)   Encephalitis, Arbovirus [MESH:D004671] (78)   West Nile Fever [MESH:D014901] (73)  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)   Arenaviridae Infections [MESH:D001117] (204)   Lassa Fever [MESH:D007835] (38)  Encephalitis, Arbovirus [MESH:D004671] (78)   West Nile Fever [MESH:D014901] (73)  Flaviviridae Infections [MESH:D018178] (1656)   Flavivirus Infections [MESH:D018177] (159)   West Nile Fever [MESH:D014901] (73)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Hemorrhagic Fevers, Viral [MESH:D006482] (102)   Lassa Fever [MESH:D007835] (38)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Enterovirus Infections [MESH:D004769] (241)   Coxsackievirus Infections [MESH:D003384] (194)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   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)   HIV Wasting Syndrome [MESH:D019247] (1956)  Skin Diseases, Viral [MESH:D017193] (203)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Tumor Virus Infections [MESH:D014412] (1069)   Papillomavirus Infections [MESH:D030361] (537)  Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  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, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Malaria [MESH:D008288] (2175)   Malaria, Falciparum [MESH:D016778] (438)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  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)  Lymphatic Vessel Tumors [MESH:D018190] (171)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  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, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Mixed Tumor, Mullerian [MESH:D018200] (64)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Rhabdoid Tumor [MESH:D018335] (61)   Rhabdoid Tumor Predisposition Syndrome 2 [MESH:C567643] (43)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Chondroma [MESH:D002812] (155)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Aggressive [MESH:D018222] (1562)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  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)  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)   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)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Large Cell [MESH:D018287] (211)  Carcinoma, Lewis Lung [MESH:D018827] (248)  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)  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, 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)  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, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Ependymoma [MESH:D004806] (76)  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)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioma, capillary infantile [MESH:C535860] (190)  Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)   Uveal melanoma [MESH:C536494] (109)  Nevus [MESH:D009506] (340)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  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)   Rectal Neoplasms [MESH:D012004] (717)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Testicular Neoplasms [MESH:D013736] (520)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   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)  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)  Thyroid Neoplasms [MESH:D013964] (2040)  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)   Laryngeal Neoplasms [MESH:D007822] (68)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  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)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Thoracic Neoplasms [MESH:D013899] (6032)   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)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neoplasms, Experimental [MESH:D009374] (5218)   Carcinoma, Lewis Lung [MESH:D018827] (248)  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)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  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)   Hemangioma, capillary infantile [MESH:C535860] (190)  Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Warts [MESH:D014860] (167)   WHIM syndrome [MESH:C536697] (148) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Osteitis Deformans [MESH:D010001] (287)  Bone Diseases, Developmental [MESH:D001848] (3315)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Dwarfism [MESH:D004392] (778)   Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Dysostoses [MESH:D004413] (1019)   Rubinstein-Taybi Syndrome [MESH:D012415] (149)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Synostosis [MESH:D013580] (817)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Oculopalatoskeletal syndrome [MESH:C537738] (45)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Osteochondrodysplasias [MESH:D010009] (2440)   Spondyloenchondrodysplasia [MESH:C535782] (71)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Spondyloepimetaphyseal Dysplasia, Pakistani Type [MESH:C567551] (63)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Enchondromatosis [MESH:D004687] (170)  Langer-Giedion Syndrome [MESH:D015826] (25)  Fibrous Dysplasia of Bone [MESH:D005357] (737)   Fibrous Dysplasia, Polyostotic [MESH:D005359] (82)  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)  Bone Diseases, Infectious [MESH:D001850] (90)   Osteomyelitis [MESH:D010019] (69)   Majeed syndrome [MESH:C537839] (33)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  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)  Bone Resorption [MESH:D001862] (2352)   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)  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)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Dysgnathia complex [MESH:C537996] (33)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Joint Diseases [MESH:D007592] (4657)   Cushing's symphalangism [MESH:C536223] (42)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Arthritis, Infectious [MESH:D001170] (1702)   Pyogenic arthritis, pyoderma gangrenosum, and acne [MESH:C536253] (15)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Contracture [MESH:D003286] (296)   Stiff Skin Syndrome [MESH:C566112] (62)  Muscular Diseases [MESH:D009135] (4071)   Compartment Syndromes [MESH:D003161] (80)  Muscle Spasticity [MESH:D009128] (187)  Contracture [MESH:D003286] (303)   Stiff Skin Syndrome [MESH:C566112] (62)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)   Facioscapulohumeral Muscular Dystrophy 1B [MESH:C563557] (13)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Rhabdomyolysis [MESH:D012206] (465)   Myoglobinuria [MESH:D009212] (96)   Myoglobinuria, Acute Recurrent, Autosomal Recessive [MESH:C564832] (64)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Hennekam lymphangiectasia lymphedema syndrome [MESH:C537255] (14)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Costello Syndrome [MESH:D056685] (407)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Oculopalatoskeletal syndrome [MESH:C537738] (45)  Holoprosencephaly [MESH:D016142] (218)   Dysgnathia complex [MESH:C537996] (33)  Holoprosencephaly 3 [MESH:C564181] (50)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Dysgnathia complex [MESH:C537996] (33)  Retrognathia [MESH:D063173] (110)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Microcephaly [MESH:D008831] (700)   Mowat-Wilson syndrome [MESH:C536990] (37)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Oculopalatoskeletal syndrome [MESH:C537738] (45)  Hip Dislocation, Congenital [MESH:D006618] (56)   Carnevale syndrome [MESH:C535586] (45)  Limb Deformities, Congenital [MESH:D017880] (1813)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Brachydactyly [MESH:D059327] (220)  Arachnodactyly [MESH:D054119] (126)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Ectromelia [MESH:D004480] (108)   Al Awadi syndrome [MESH:C535612] (30)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  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)   Coffin-Siris syndrome [MESH:C536436] (102)  NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Synostosis [MESH:D013580] (817)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Oculopalatoskeletal syndrome [MESH:C537738] (45)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Rheumatoid [MESH:D001172] (3603)  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)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  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)   Currarino triad [MESH:C536221] (47)  Barrett Esophagus [MESH:D001471] (1930)  Anus, Imperforate [MESH:D001006] (140)   VATER association [MESH:C536534] (46)  Esophageal Atresia [MESH:D004933] (47)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Hirschsprung Disease [MESH:D006627] (361)   Mowat-Wilson syndrome [MESH:C536990] (37)  Digestive System Fistula [MESH:D016154] (102)   Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  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)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Deglutition Disorders [MESH:D003680] (1538)   Esophageal Motility Disorders [MESH:D015154] (1489)   Gastroesophageal Reflux [MESH:D005764] (1465)  Esophageal Atresia [MESH:D004933] (47)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Esophagitis [MESH:D004941] (1120)   Esophagitis, Peptic [MESH:D004942] (709)  Gastroenteritis [MESH:D005759] (4066)   Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enteritis [MESH:D004751] (157)   Ileitis [MESH:D007079] (137)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Esophagitis [MESH:D004941] (1120)   Esophagitis, Peptic [MESH:D004942] (709)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 28, Autosomal Recessive [MESH:C567728] (43)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  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)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)   Mowat-Wilson syndrome [MESH:C536990] (37)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)  Enteritis [MESH:D004751] (157)   Ileitis [MESH:D007079] (137)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Ileal Diseases [MESH:D007077] (143)   Ileitis [MESH:D007079] (137)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 28, Autosomal Recessive [MESH:C567728] (43)  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)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Intestinal Polyposis [MESH:D044483] (1610)   Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Malabsorption Syndromes [MESH:D008286] (492)   Glucose-Galactose Malabsorption [MESH:C562602] (49)  Celiac Disease [MESH:D002446] (340)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Esophagitis, Peptic [MESH:D004942] (709)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Budd-Chiari Syndrome [MESH:D006502] (164)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatorenal Syndrome [MESH:D006530] (910)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  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)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Dysgnathia complex [MESH:C537996] (33)  External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation [MESH:C566509] (71)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mandibular Diseases [MESH:D008336] (450)   Retrognathia [MESH:D063173] (110)   Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (98)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   PCI 5002 [MESH:C568608] (433)  Mouth Abnormalities [MESH:D009056] (1383)   Contractures, Congenital, Torticollis, and Malignant Hyperthermia [MESH:C565679] (34)  Cleft Lip [MESH:D002971] (914)   PCI 5002 [MESH:C568608] (433)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  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)  Gingival Diseases [MESH:D005882] (217)   Gingival Overgrowth [MESH:D019214] (192)   Gingival Hyperplasia [MESH:D005885] (161)  Periodontitis [MESH:D010518] (843)   Periodontitis, Aggressive, 2 [MESH:C566946] (310)  Aggressive Periodontitis [MESH:D010520] (74)  Chronic Periodontitis [MESH:D055113] (231)  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 teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Dysgnathia complex [MESH:C537996] (33)  External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation [MESH:C566509] (71)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Retrognathia [MESH:D063173] (110)   Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (98)  Mouth Abnormalities [MESH:D009056] (1383)   Contractures, Congenital, Torticollis, and Malignant Hyperthermia [MESH:C565679] (34)  Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 12 [MESH:C567548] (434)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Respiratory System Abnormalities [MESH:D015619] (243)  Thoracic Diseases [MESH:D013896] (81)  Bronchial Diseases [MESH:D001982] (4382)   Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Ciliary Motility Disorders [MESH:D002925] (104)   Ciliary Dyskinesia, Primary, 12 [MESH:C567211] (11)  Laryngeal Diseases [MESH:D007818] (215)   Laryngeal Neoplasms [MESH:D007822] (68)  Lung Diseases [MESH:D008171] (7249)   Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Veno-Occlusive Disease [MESH:D011668] (55)  Hypertension, Pulmonary [MESH:D006976] (2000)   Pulmonary arterial hypertension [MESH:C536282] (94)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Surfactant Metabolism Dysfunction, Pulmonary, 1 [MESH:C566882] (102)  Idiopathic Interstitial Pneumonias [MESH:D054988] (314)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  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)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   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)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  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)  Pulmonary Alveolar Proteinosis [MESH:D011649] (139)   Surfactant Metabolism Dysfunction, Pulmonary, 1 [MESH:C566882] (102)  Pulmonary Fibrosis [MESH:D011658] (3140)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Nose Diseases [MESH:D009668] (1504)   Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Hyperventilation [MESH:D006985] (654)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Respiratory Insufficiency [MESH:D012131] (841)   Hypoventilation [MESH:D007040] (360)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Respiratory Tract Fistula [MESH:D016156] (91)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Laryngeal Neoplasms [MESH:D007822] (68)  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)  Tracheal Diseases [MESH:D014133] (107)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ciliary Motility Disorders [MESH:D002925] (104)   Ciliary Dyskinesia, Primary, 12 [MESH:C567211] (11)  Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Deaf-Blind Disorders [MESH:D054062] (132)   Wolfram Syndrome [MESH:D014929] (37)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Chudley-Mccullough syndrome [MESH:C535459] (45)  Donnai-Barrow syndrome [MESH:C536390] (40)  Thiamine responsive megaloblastic anemia syndrome [MESH:C536510] (39)  Pendred syndrome [MESH:C536648] (35)  Barakat syndrome [MESH:C537907] (71)  Deafness, Autosomal Recessive 12 [MESH:C563327] (46)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Laryngeal Diseases [MESH:D007818] (211)   Laryngeal Neoplasms [MESH:D007822] (68)  Nose Diseases [MESH:D009668] (1504)   Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Laryngeal Neoplasms [MESH:D007822] (68)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Restless Legs Syndrome [MESH:D012148] (379)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Aicardi-Goutieres syndrome 5 [MESH:C535608] (22)  Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)  Central Nervous System Diseases [MESH:D002493] (9745)   Endocrine-Cerebroosteodysplasia [MESH:C567210] (26)  Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)  Hepatolenticular Degeneration [MESH:D006527] (473)  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)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  MERRF Syndrome [MESH:D017243] (1053)  Tyrosinemias [MESH:D020176] (132)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Episodic Ataxia, Type 6 [MESH:C567207] (70)  Spinocerebellar Ataxias [MESH:D020754] (406)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   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)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)   Frontotemporal Dementia [MESH:D057180] (300)   Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Encephalitis [MESH:D004660] (226)   Meningoencephalitis [MESH:D008590] (179)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsy, Juvenile [MESH:D020190] (166)  Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Complex Partial [MESH:D017029] (43)  Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  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)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Leukoencephalopathies [MESH:D056784] (1916)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Central Nervous System Infections [MESH:D002494] (1823)   Meningoencephalitis [MESH:D008590] (207)  Central Nervous System Viral Diseases [MESH:D020805] (1416)   Encephalitis [MESH:D004660] (226)   Encephalitis, Viral [MESH:D018792] (183)   Encephalitis, Arbovirus [MESH:D004671] (78)   West Nile Fever [MESH:D014901] (73)  Encephalitis [MESH:D004660] (351)   Meningoencephalitis [MESH:D008590] (179)  Encephalitis, Viral [MESH:D018792] (183)   Encephalitis, Arbovirus [MESH:D004671] (78)   West Nile Fever [MESH:D014901] (73)  Meningitis [MESH:D008581] (1506)   Meningoencephalitis [MESH:D008590] (179)  Meningitis [MESH:D008581] (352)   Meningoencephalitis [MESH:D008590] (179)  Movement Disorders [MESH:D009069] (4823)   Angelman Syndrome [MESH:D017204] (124)  Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Paroxysmal nonkinesigenic dyskinesia [MESH:C537181] (23)  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)  Ocular Motility Disorders [MESH:D015835] (364)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 8 [MESH:C563895] (17)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant [MESH:C566672] (17)  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)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Syringomyelia [MESH:D013595] (50)   Currarino triad [MESH:C536221] (47)  Chronobiology Disorders [MESH:D021081] (970)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (93)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Strabismus [MESH:D013285] (79)   Carnevale syndrome [MESH:C535586] (45)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Wolfram Syndrome [MESH:D014929] (37)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Multiple Sclerosis [MESH:D009103] (1716)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Nervous System Malformations [MESH:D009421] (3354)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Aicardi-Goutieres syndrome 5 [MESH:C535608] (22)  Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Donnai-Barrow syndrome [MESH:C536390] (40)  Holoprosencephaly [MESH:D016142] (218)   Dysgnathia complex [MESH:C537996] (33)  Holoprosencephaly 3 [MESH:C564181] (50)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Mowat-Wilson syndrome [MESH:C536990] (37)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Neural Tube Defects [MESH:D009436] (2143)   Meningomyelocele [MESH:D008591] (100)  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)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neurodegenerative Diseases [MESH:D019636] (6613)   Familial apoceruloplasmin deficiency [MESH:C536004] (211)  Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)  Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Wolfram Syndrome [MESH:D014929] (37)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 8 [MESH:C563895] (17)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant [MESH:C566672] (17)  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)  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 8 [MESH:C563895] (17)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)   Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Paresis [MESH:D010291] (419)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Episodic Ataxia, Type 6 [MESH:C567207] (70)  Spinocerebellar Ataxias [MESH:D020754] (406)  Chorea [MESH:D002819] (189)   Paroxysmal nonkinesigenic dyskinesia [MESH:C537181] (23)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Memory Disorders [MESH:D008569] (3233)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)   Aphasia [MESH:D001037] (219)  Intellectual Disability [MESH:D008607] (3054)   Coffin-Siris syndrome [MESH:C536436] (102)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Down Syndrome [MESH:D004314] (1287)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  Williams Syndrome [MESH:D018980] (133)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Adrenoleukodystrophy [MESH:D000326] (1348)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Spasticity [MESH:D009128] (187)  Pain [MESH:D010146] (3875)   Pain, Intractable [MESH:D010148] (707)  Back Pain [MESH:D001416] (287)   Low Back Pain [MESH:D017116] (244)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5011)   Olfaction Disorders [MESH:D000857] (105)  Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Deaf-Blind Disorders [MESH:D054062] (132)   Wolfram Syndrome [MESH:D014929] (37)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Chudley-Mccullough syndrome [MESH:C535459] (45)  Donnai-Barrow syndrome [MESH:C536390] (40)  Thiamine responsive megaloblastic anemia syndrome [MESH:C536510] (39)  Pendred syndrome [MESH:C536648] (35)  Barakat syndrome [MESH:C537907] (71)  Deafness, Autosomal Recessive 12 [MESH:C563327] (46)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (501)   Blindness [MESH:D001766] (252)   Deaf-Blind Disorders [MESH:D054062] (132)   Wolfram Syndrome [MESH:D014929] (37)  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 8 [MESH:C563895] (17)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant [MESH:C566672] (17)  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)   Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant [MESH:C566672] (17)  Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Diseases [MESH:D009135] (3538)   Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)   Facioscapulohumeral Muscular Dystrophy 1B [MESH:C563557] (13)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Mononeuropathies [MESH:D020422] (604)   Sciatic Neuropathy [MESH:D020426] (477)  Neuralgia [MESH:D009437] (2078)   Neuralgia, Postherpetic [MESH:D051474] (742)  Polyneuropathies [MESH:D011115] (1134)   Tangier Disease [MESH:D013631] (170)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  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, Circadian Rhythm [MESH:D020178] (94)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82)  Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Restless Legs Syndrome [MESH:D012148] (379)  Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Parasomnias [MESH:D020447] (453)   Restless Legs Syndrome [MESH:D012148] (379)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Corneal Diseases [MESH:D003316] (1445)   Keratoconus [MESH:D007640] (121)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Corneal Opacity [MESH:D003318] (544)   Peters anomaly [MESH:C537884] (465)  Eye Abnormalities [MESH:D005124] (1233)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Peters anomaly [MESH:C537884] (465)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anophthalmos [MESH:D000853] (63)  Ectopia Lentis [MESH:D004479] (73)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Coloboma [MESH:D003103] (315)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Graves Ophthalmopathy [MESH:D049970] (165)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Leber Congenital Amaurosis [MESH:D057130] (157)   Leber Congenital Amaurosis 14 [MESH:C567636] (41)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Wolfram Syndrome [MESH:D014929] (37)  Retinitis Pigmentosa [MESH:D012174] (414)   Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Leber Congenital Amaurosis 14 [MESH:C567636] (41)  Eye Neoplasms [MESH:D005134] (413)   Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Eyelid Diseases [MESH:D005141] (882)   Blepharoptosis [MESH:D001763] (117)   Carnevale syndrome [MESH:C535586] (45)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Cataract, Pulverulent, Juvenile-Onset [MESH:C565703] (69)  Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Lens Subluxation [MESH:D007906] (74)   Ectopia Lentis [MESH:D004479] (73)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma 3, Primary Congenital, A [MESH:C565547] (434)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  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)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Strabismus [MESH:D013285] (79)   Carnevale syndrome [MESH:C535586] (45)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Wolfram Syndrome [MESH:D014929] (37)  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)   MASS syndrome [MESH:C536030] (62)  Donnai-Barrow syndrome [MESH:C536390] (40)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Vein Occlusion [MESH:D012170] (607)  Leber Congenital Amaurosis [MESH:D057130] (157)   Leber Congenital Amaurosis 14 [MESH:C567636] (41)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Stargardt disease 4 [MESH:C535521] (63)  Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Leber Congenital Amaurosis 14 [MESH:C567636] (41)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Uveal Diseases [MESH:D014603] (2428)   Iris Diseases [MESH:D007499] (348)   Exfoliation Syndrome [MESH:D017889] (48)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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)  Vision Disorders [MESH:D014786] (534)   Blindness [MESH:D001766] (259)   Deaf-Blind Disorders [MESH:D054062] (132)   Wolfram Syndrome [MESH:D014929] (37) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Hennekam lymphangiectasia lymphedema syndrome [MESH:C537255] (14)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)  Penile Diseases [MESH:D010409] (1805)   Penile Neoplasms [MESH:D010412] (890)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  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)   Carnevale syndrome [MESH:C535586] (45)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Urogenital Abnormalities [MESH:D014564] (2065)   Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Hyperandrogenism [MESH:D017588] (98)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Denys-Drash Syndrome [MESH:D030321] (57)  Frasier Syndrome [MESH:D052159] (57)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Hyperandrogenism [MESH:D017588] (98)  Gonadal Dysgenesis [MESH:D006059] (492)   Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Diabetes Insipidus [MESH:D003919] (354)   Wolfram Syndrome [MESH:D014929] (37)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Barakat syndrome [MESH:C537907] (71)  Nephrotic Syndrome [MESH:D009404] (1536)   Nephrotic syndrome, idiopathic, steroid-resistant [MESH:C536404] (30)  Renal Insufficiency [MESH:D051437] (4951)   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)   Frasier Syndrome [MESH:D052159] (57)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Donnai-Barrow syndrome [MESH:C536390] (40)  Pseudohypoaldosteronism [MESH:D011546] (232)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Renal Aminoacidurias [MESH:D000608] (95)   Cystinuria [MESH:D003555] (67)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Vesico-Ureteral Reflux [MESH:D014718] (58)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455) 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)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  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)   Endometrial Hyperplasia [MESH:D004714] (263)  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)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Hyperandrogenism [MESH:D017588] (98)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Denys-Drash Syndrome [MESH:D030321] (57)  Frasier Syndrome [MESH:D052159] (57)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Hyperandrogenism [MESH:D017588] (98)  Gonadal Dysgenesis [MESH:D006059] (492)   Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  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)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Diabetes Insipidus [MESH:D003919] (354)   Wolfram Syndrome [MESH:D014929] (37)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Barakat syndrome [MESH:C537907] (71)  Nephrotic Syndrome [MESH:D009404] (1536)   Nephrotic syndrome, idiopathic, steroid-resistant [MESH:C536404] (30)  Renal Insufficiency [MESH:D051437] (4951)   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)   Frasier Syndrome [MESH:D052159] (57)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Donnai-Barrow syndrome [MESH:C536390] (40)  Pseudohypoaldosteronism [MESH:D011546] (232)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Renal Aminoacidurias [MESH:D000608] (95)   Cystinuria [MESH:D003555] (67)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Vesico-Ureteral Reflux [MESH:D014718] (58)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Fetal Death [MESH:D005313] (464)  Placenta Diseases [MESH:D010922] (1781)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Fetal Diseases [MESH:D005315] (1206)   Erythroblastosis, Fetal [MESH:D004899] (24)   Hydrops Fetalis [MESH:D015160] (23)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Fetal Membranes, Premature Rupture [MESH:D005322] (356)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) 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)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Malpuech facial clefting syndrome [MESH:C535704] (45)  VATER association [MESH:C536534] (46)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Vascular Malformations [MESH:D054079] (1098)   Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Heart Diseases [MESH:D006331] (8614)   Cardiac Tamponade [MESH:D002305] (175)  Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Pericardial Effusion [MESH:D010490] (1015)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Tachycardia [MESH:D013610] (3339)  Ventricular Fibrillation [MESH:D014693] (624)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial Fibrillation, Familial, 3 [MESH:C563817] (60)  Atrial Fibrillation, Familial, 4 [MESH:C566244] (20)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 3 [MESH:C567509] (44)  Brugada Syndrome 7 [MESH:C567734] (31)  Long QT Syndrome [MESH:D008133] (693)   Timothy syndrome [MESH:C536962] (44)  Long Qt Syndrome 6 [MESH:C566333] (20)  Long Qt Syndrome 11 [MESH:C567513] (48)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1C [MESH:C563307] (20)  Cardiomyopathy, Dilated, 1w [MESH:C566954] (66)  Cardiomyopathy, Dilated, 1BB [MESH:C567877] (31)  Cardiomyopathies [MESH:D009202] (5331)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Endomyocardial Fibrosis [MESH:D004719] (521)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1C [MESH:C563307] (20)  Cardiomyopathy, Dilated, 1w [MESH:C566954] (66)  Cardiomyopathy, Dilated, 1BB [MESH:C567877] (31)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 15 [MESH:C567681] (66)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Malpuech facial clefting syndrome [MESH:C535704] (45)  VATER association [MESH:C536534] (46)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Aortic Stenosis, Supravalvular [MESH:D021921] (135)   Williams Syndrome [MESH:D018980] (133)  Heart Valve Prolapse [MESH:D016127] (99)   Mitral Valve Prolapse [MESH:D008945] (96)   MASS syndrome [MESH:C536030] (62)  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, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Thrombosis [MESH:D003328] (255)  Coronary Vasospasm [MESH:D003329] (533)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Coronary Artery Disease, Autosomal Dominant 2 [MESH:C567045] (24)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Coronary Artery Disease, Autosomal Dominant 2 [MESH:C567045] (24)  Myocardial Stunning [MESH:D017682] (1816)  Shock, Cardiogenic [MESH:D012770] (269)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Stenosis, Supravalvular [MESH:D021921] (50)  Vascular Diseases [MESH:D014652] (8691)   Angioedema [MESH:D000799] (837)  Arteritis [MESH:D001167] (1084)  Compartment Syndromes [MESH:D003161] (80)  Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Pulmonary Veno-Occlusive Disease [MESH:D011668] (55)  Retinal Vein Occlusion [MESH:D012170] (607)  Superior Vena Cava Syndrome [MESH:D013479] (64)  Varicose Veins [MESH:D014648] (383)  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)  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)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Coronary Artery Disease, Autosomal Dominant 2 [MESH:C567045] (24)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   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)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Embolism, Fat [MESH:D004620] (261)   Embolism, Cholesterol [MESH:D017700] (255)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Thrombosis [MESH:D013927] (3101)   Coronary Thrombosis [MESH:D003328] (255)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Venous Thrombosis [MESH:D020246] (1141)   Budd-Chiari Syndrome [MESH:D006502] (164)  Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Occipital horn syndrome [MESH:C537860] (58)  Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  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, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Thrombosis [MESH:D003328] (255)  Coronary Vasospasm [MESH:D003329] (533)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Coronary Artery Disease, Autosomal Dominant 2 [MESH:C567045] (24)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Coronary Artery Disease, Autosomal Dominant 2 [MESH:C567045] (24)  Myocardial Stunning [MESH:D017682] (1816)  Shock, Cardiogenic [MESH:D012770] (269)  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)   Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Hemolytic [MESH:D000743] (3083)   Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to [MESH:C565545] (88)  Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to [MESH:C565557] (312)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)   Majeed syndrome [MESH:C537839] (33)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Anemia, Macrocytic [MESH:D000748] (382)   5q- syndrome [MESH:C535323] (131)  Anemia, Megaloblastic [MESH:D000749] (288)   Thiamine responsive megaloblastic anemia syndrome [MESH:C536510] (39)  Anemia, Sideroblastic [MESH:D000756] (636)   X-linked sideroblastic anemia [MESH:C536761] (58)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Factor V Deficiency [MESH:D005166] (61)  Factor XIII Deficiency [MESH:D005177] (52)  Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Coagulation Protein Disorders [MESH:D020147] (580)   Factor V Deficiency [MESH:D005166] (61)  Factor XIII Deficiency [MESH:D005177] (52)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Hydrops Fetalis [MESH:D015160] (23)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Dysgammaglobulinemia [MESH:D004406] (67)   IgA Deficiency [MESH:D017098] (45)   Immunoglobulin a deficiency 2 [MESH:C536291] (7)  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)  Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)   X-linked sideroblastic anemia [MESH:C536761] (58)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  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)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Hydrops Fetalis [MESH:D015160] (23)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Factor V Deficiency [MESH:D005166] (61)  Factor XIII Deficiency [MESH:D005177] (52)  Thrombocythemia, Essential [MESH:D013920] (707)  Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Occipital horn syndrome [MESH:C537860] (58)  Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Leukocyte Disorders [MESH:D007960] (2662)   Neutrophilia, Hereditary [MESH:C563010] (32)  Leukocytosis [MESH:D007964] (988)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)   Neutropenia, Severe Congenital, X-Linked [MESH:C564539] (27)  Lymphopenia [MESH:D008231] (990)   Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Chediak-Higashi Syndrome [MESH:D002609] (21)  Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Thrombophilia [MESH:D019851] (592)   Thrombophilia, hereditary [MESH:C540694] (59)  Disseminated Intravascular Coagulation [MESH:D004211] (462)  Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Lymphatic Diseases [MESH:D008206] (5167)   Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Lymphohistiocytosis, Hemophagocytic [MESH:D051359] (76)   Hemophagocytic lymphohistiocytosis, familial, 2 [MESH:C537250] (38)  Hemophagocytic lymphohistiocytosis, familial, 4 [MESH:C537252] (29)  Lymphangiectasis [MESH:D008200] (20)   Lymphangiectasis, Intestinal [MESH:D008201] (18)   Hennekam lymphangiectasia lymphedema syndrome [MESH:C537255] (14)  Lymphatic Abnormalities [MESH:D044148] (251)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Lymphangiectasis, Intestinal [MESH:D008201] (18)   Hennekam lymphangiectasia lymphedema syndrome [MESH:C537255] (14)  Lymphedema [MESH:D008209] (162)   Hennekam lymphangiectasia lymphedema syndrome [MESH:C537255] (14)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 [MESH:C567815] (14)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  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, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  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)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Coffin-Siris syndrome [MESH:C536436] (102)  Angelman Syndrome [MESH:D017204] (124)  Bardet-Biedl Syndrome [MESH:D020788] (110)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Costello Syndrome [MESH:D056685] (407)  Down Syndrome [MESH:D004314] (1287)  Incontinentia Pigmenti [MESH:D007184] (57)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Wolfram Syndrome [MESH:D014929] (37)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Deaf-Blind Disorders [MESH:D054062] (132)   Wolfram Syndrome [MESH:D014929] (37)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Holoprosencephaly [MESH:D016142] (218)   Dysgnathia complex [MESH:C537996] (33)  Holoprosencephaly 3 [MESH:C564181] (50)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Waardenburg Syndrome [MESH:D014849] (243)   ABCD syndrome [MESH:C535334] (143)  Waardenburg Syndrome, Type 2D [MESH:C563839] (48)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Malpuech facial clefting syndrome [MESH:C535704] (45)  VATER association [MESH:C536534] (46)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 [MESH:C565707] (31)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  Long QT Syndrome [MESH:D008133] (693)   Timothy syndrome [MESH:C536962] (44)  Long Qt Syndrome 6 [MESH:C566333] (20)  Long Qt Syndrome 11 [MESH:C567513] (48)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Chromosome Disorders [MESH:D025063] (2030)   Angelman Syndrome [MESH:D017204] (124)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Down Syndrome [MESH:D004314] (1287)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  Williams Syndrome [MESH:D018980] (133)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Holoprosencephaly [MESH:D016142] (218)   Dysgnathia complex [MESH:C537996] (33)  Holoprosencephaly 3 [MESH:C564181] (50)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Digestive System Abnormalities [MESH:D004065] (507)   Currarino triad [MESH:C536221] (47)  Anus, Imperforate [MESH:D001006] (140)   VATER association [MESH:C536534] (46)  Esophageal Atresia [MESH:D004933] (47)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Hirschsprung Disease [MESH:D006627] (361)   Mowat-Wilson syndrome [MESH:C536990] (37)  Eye Abnormalities [MESH:D005124] (1233)   Oculopalatoskeletal syndrome [MESH:C537738] (45)  Peters anomaly [MESH:C537884] (465)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anophthalmos [MESH:D000853] (63)  Ectopia Lentis [MESH:D004479] (73)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Coloboma [MESH:D003103] (315)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Lymphatic Abnormalities [MESH:D044148] (251)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Lymphangiectasis, Intestinal [MESH:D008201] (18)   Hennekam lymphangiectasia lymphedema syndrome [MESH:C537255] (14)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Hennekam lymphangiectasia lymphedema syndrome [MESH:C537255] (14)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Oculopalatoskeletal syndrome [MESH:C537738] (45)  Holoprosencephaly [MESH:D016142] (218)   Dysgnathia complex [MESH:C537996] (33)  Holoprosencephaly 3 [MESH:C564181] (50)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Dysgnathia complex [MESH:C537996] (33)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Microcephaly [MESH:D008831] (700)   Mowat-Wilson syndrome [MESH:C536990] (37)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Oculopalatoskeletal syndrome [MESH:C537738] (45)  Hip Dislocation, Congenital [MESH:D006618] (56)   Carnevale syndrome [MESH:C535586] (45)  Limb Deformities, Congenital [MESH:D017880] (1813)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Brachydactyly [MESH:D059327] (220)  Lower Extremity Deformities, Congenital [MESH:D038061] (81)  Arachnodactyly [MESH:D054119] (126)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Ectromelia [MESH:D004480] (108)   Al Awadi syndrome [MESH:C535612] (30)  Foot Deformities, Congenital [MESH:D005532] (538)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Synostosis [MESH:D013580] (817)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Oculopalatoskeletal syndrome [MESH:C537738] (45)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Nervous System Malformations [MESH:D009421] (3354)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Aicardi-Goutieres syndrome 5 [MESH:C535608] (22)  Microphthalmia, Syndromic 3 [MESH:C565948] (43)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Donnai-Barrow syndrome [MESH:C536390] (40)  Holoprosencephaly [MESH:D016142] (218)   Dysgnathia complex [MESH:C537996] (33)  Holoprosencephaly 3 [MESH:C564181] (50)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Holoprosencephaly [MESH:D016142] (218)   Dysgnathia complex [MESH:C537996] (33)  Holoprosencephaly 3 [MESH:C564181] (50)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Mowat-Wilson syndrome [MESH:C536990] (37)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Neural Tube Defects [MESH:D009436] (2143)   Meningomyelocele [MESH:D008591] (100)  Skin Abnormalities [MESH:D012868] (1723)   Incontinentia Pigmenti [MESH:D007184] (57)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Occipital horn syndrome [MESH:C537860] (58)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Dysgnathia complex [MESH:C537996] (33)  Retrognathia [MESH:D063173] (110)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Urogenital Abnormalities [MESH:D014564] (2064)   Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Hyperandrogenism [MESH:D017588] (98)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Denys-Drash Syndrome [MESH:D030321] (57)  Frasier Syndrome [MESH:D052159] (57)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Hyperandrogenism [MESH:D017588] (98)  Gonadal Dysgenesis [MESH:D006059] (492)   Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Fetal Diseases [MESH:D005315] (1205)   Erythroblastosis, Fetal [MESH:D004899] (24)   Hydrops Fetalis [MESH:D015160] (23)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Costello Syndrome [MESH:D056685] (407)  Frasier Syndrome [MESH:D052159] (57)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)   Majeed syndrome [MESH:C537839] (33)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Factor V Deficiency [MESH:D005166] (61)  Factor XIII Deficiency [MESH:D005177] (52)  Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 3 [MESH:C567509] (44)  Brugada Syndrome 7 [MESH:C567734] (31)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 15 [MESH:C567681] (66)  Chromosome Disorders [MESH:D025063] (2030)   Angelman Syndrome [MESH:D017204] (124)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Down Syndrome [MESH:D004314] (1287)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  Williams Syndrome [MESH:D018980] (133)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Holoprosencephaly [MESH:D016142] (218)   Dysgnathia complex [MESH:C537996] (33)  Holoprosencephaly 3 [MESH:C564181] (50)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Dwarfism [MESH:D004392] (783)   Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Weill-Marchesani Syndrome [MESH:D056846] (65)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Wolfram Syndrome [MESH:D014929] (37)  Retinitis Pigmentosa [MESH:D012174] (442)   Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Leber Congenital Amaurosis 14 [MESH:C567636] (41)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  X-linked sideroblastic anemia [MESH:C536761] (58)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Neutropenia, Severe Congenital, X-Linked [MESH:C564539] (27)  Atypical Mycobacteriosis, Familial, X-Linked 1 [MESH:C567070] (56)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Wiskott-Aldrich Syndrome [MESH:D014923] (28)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Adrenoleukodystrophy [MESH:D000326] (1348)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Hydrops Fetalis [MESH:D015160] (23)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Adrenoleukodystrophy [MESH:D000326] (1348)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Wolfram Syndrome [MESH:D014929] (37)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Trimethylaminuria [MESH:C536561] (61)  Xanthinuria, Type I [MESH:C562584] (190)  Porphyrias [MESH:D011164] (917)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutamine deficiency, congenital [MESH:C536832] (117)  Glutathione synthetase deficiency [MESH:C536835] (88)  Glutathionuria [MESH:C536836] (96)  Methylmalonic acidemia [MESH:C537358] (764)  Acidemia, isovaleric [MESH:C538167] (47)  Hyperprolinemia [MESH:C538384] (45)  Glycine N-Methyltransferase Deficiency [MESH:C564683] (72)  Maple Syrup Urine Disease [MESH:D008375] (127)  Tyrosinemias [MESH:D020176] (132)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Hyperhomocysteinemia [MESH:D020138] (1724)   Gamma-cystathionase deficiency [MESH:C535408] (106)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  MERRF Syndrome [MESH:D017243] (1053)  Tyrosinemias [MESH:D020176] (132)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Glucose-Galactose Malabsorption [MESH:C562602] (49)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease Type IV [MESH:D006011] (56)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (365)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, type 4 [MESH:C537249] (89)  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)   Adrenoleukodystrophy [MESH:D000326] (1348)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Donnai-Barrow syndrome [MESH:C536390] (40)  Pseudohypoaldosteronism [MESH:D011546] (232)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Renal Aminoacidurias [MESH:D000608] (95)   Cystinuria [MESH:D003555] (67)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Lathosterolosis [MESH:C537880] (66)  Mineralocorticoid Excess Syndrome, Apparent [MESH:D043204] (121)   Apparent mineralocorticoid excess [MESH:C537422] (120)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)   Facioscapulohumeral Muscular Dystrophy 1B [MESH:C563557] (13)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Polyposis Syndrome, Hereditary Mixed, 2 [MESH:C566451] (26)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Skin Diseases, Genetic [MESH:D012873] (3456)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Stiff Skin Syndrome [MESH:C566112] (62)  Dermatitis, Atopic [MESH:D003876] (2052)  Incontinentia Pigmenti [MESH:D007184] (57)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Cutis Laxa [MESH:D003483] (177)   Occipital horn syndrome [MESH:C537860] (58)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Occipital horn syndrome [MESH:C537860] (58)  Epidermolysis Bullosa [MESH:D004820] (259)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Papillon-Lefevre Disease [MESH:D010214] (76)   Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Hernia, Umbilical [MESH:D006554] (115)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Cutaneous [MESH:D008178] (65)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Occipital horn syndrome [MESH:C537860] (58)  Cutis Laxa [MESH:D003483] (177)   Occipital horn syndrome [MESH:C537860] (58)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   MASS syndrome [MESH:C536030] (62)  Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Cutaneous [MESH:D008178] (65)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Acne Vulgaris [MESH:D000152] (61)   Pyogenic arthritis, pyoderma gangrenosum, and acne [MESH:C536253] (15)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Drug Eruptions [MESH:D003875] (2697)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Acne Vulgaris [MESH:D000152] (61)   Pyogenic arthritis, pyoderma gangrenosum, and acne [MESH:C536253] (15)  Hair Diseases [MESH:D006201] (1891)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)  Keratosis [MESH:D007642] (1941)   Keratoderma, Palmoplantar [MESH:D007645] (287)   Papillon-Lefevre Disease [MESH:D010214] (76)   Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Pigmentation Disorders [MESH:D010859] (1215)   Cafe-au-Lait Spots [MESH:D019080] (186)  Incontinentia Pigmenti [MESH:D007184] (57)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Pyoderma [MESH:D011711] (24)   Pyoderma Gangrenosum [MESH:D017511] (22)   Pyogenic arthritis, pyoderma gangrenosum, and acne [MESH:C536253] (15)  Sebaceous Gland Diseases [MESH:D012625] (245)   Acne Vulgaris [MESH:D000152] (61)   Pyogenic arthritis, pyoderma gangrenosum, and acne [MESH:C536253] (15)  Skin Abnormalities [MESH:D012868] (1709)   Incontinentia Pigmenti [MESH:D007184] (57)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Occipital horn syndrome [MESH:C537860] (58)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Skin Diseases, Genetic [MESH:D012873] (3481)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Stiff Skin Syndrome [MESH:C566112] (62)  Dermatitis, Atopic [MESH:D003876] (2052)  Incontinentia Pigmenti [MESH:D007184] (57)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Cutis Laxa [MESH:D003483] (177)   Occipital horn syndrome [MESH:C537860] (58)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Occipital horn syndrome [MESH:C537860] (58)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Papillon-Lefevre Disease [MESH:D010214] (76)   Keratosis palmoplantaris with periodontopathia and onychogryposis [MESH:C537627] (73)  Skin Diseases, Infectious [MESH:D012874] (2684)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)   Candidiasis familial chronic mucocutaneous, autosomal recessive [MESH:C537979] (36)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Viral [MESH:D017193] (203)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  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)  Pyoderma Gangrenosum [MESH:D017511] (22)   Pyogenic arthritis, pyoderma gangrenosum, and acne [MESH:C536253] (15)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Pemphigoid, Bullous [MESH:D010391] (707)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)  Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Skin Ulcer [MESH:D012883] (229)   Pyoderma Gangrenosum [MESH:D017511] (22)   Pyogenic arthritis, pyoderma gangrenosum, and acne [MESH:C536253] (15) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Porphyrias [MESH:D011164] (917)  Acid-Base Imbalance [MESH:D000137] (854)   Acidosis [MESH:D000138] (626)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  MERRF Syndrome [MESH:D017243] (1053)  Tyrosinemias [MESH:D020176] (132)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Fanconi Anemia [MESH:D005199] (1604)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hypoglycemia [MESH:D007003] (2420)  Diabetes Mellitus [MESH:D003920] (5891)   Thiamine responsive megaloblastic anemia syndrome [MESH:C536510] (39)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 22 [MESH:C567284] (72)  Wolfram Syndrome [MESH:D014929] (37)  Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)  Iron Metabolism Disorders [MESH:D019189] (2139)   Familial apoceruloplasmin deficiency [MESH:C536004] (211)  Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, type 4 [MESH:C537249] (89)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (409)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Malabsorption Syndromes [MESH:D008286] (1869)   Glucose-Galactose Malabsorption [MESH:C562602] (49)  Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)   Gamma-cystathionase deficiency [MESH:C535408] (106)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Trimethylaminuria [MESH:C536561] (61)  Xanthinuria, Type I [MESH:C562584] (190)  Porphyrias [MESH:D011164] (917)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutamine deficiency, congenital [MESH:C536832] (117)  Glutathione synthetase deficiency [MESH:C536835] (88)  Glutathionuria [MESH:C536836] (96)  Methylmalonic acidemia [MESH:C537358] (764)  Acidemia, isovaleric [MESH:C538167] (47)  Hyperprolinemia [MESH:C538384] (45)  Glycine N-Methyltransferase Deficiency [MESH:C564683] (72)  Maple Syrup Urine Disease [MESH:D008375] (127)  Tyrosinemias [MESH:D020176] (132)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Hyperhomocysteinemia [MESH:D020138] (1724)   Gamma-cystathionase deficiency [MESH:C535408] (106)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  MERRF Syndrome [MESH:D017243] (1053)  Tyrosinemias [MESH:D020176] (132)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Glucose-Galactose Malabsorption [MESH:C562602] (49)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease Type IV [MESH:D006011] (56)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (365)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, type 4 [MESH:C537249] (89)  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)   Adrenoleukodystrophy [MESH:D000326] (1348)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Donnai-Barrow syndrome [MESH:C536390] (40)  Pseudohypoaldosteronism [MESH:D011546] (232)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Renal Aminoacidurias [MESH:D000608] (89)   Cystinuria [MESH:D003555] (67)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Lathosterolosis [MESH:C537880] (66)  Mineralocorticoid Excess Syndrome, Apparent [MESH:D043204] (121)   Apparent mineralocorticoid excess [MESH:C537422] (120)  Mitochondrial Diseases [MESH:D028361] (2561)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Proteostasis Deficiencies [MESH:D057165] (3522)   TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 8 [MESH:C563895] (17)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)   Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Starvation [MESH:D013217] (50)  Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)  Vitamin D Deficiency [MESH:D014808] (360)  Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)   Gamma-cystathionase deficiency [MESH:C535408] (106)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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)   Endocrine-Cerebroosteodysplasia [MESH:C567210] (26)  Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Insufficiency [MESH:D000309] (1599)   Addison Disease [MESH:D000224] (40)  Adrenoleukodystrophy [MESH:D000326] (1348)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Hyperaldosteronism [MESH:D006929] (419)  Diabetes Mellitus [MESH:D003920] (6159)   Thiamine responsive megaloblastic anemia syndrome [MESH:C536510] (39)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  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, 22 [MESH:C567284] (72)  Wolfram Syndrome [MESH:D014929] (37)  Dwarfism [MESH:D004392] (698)   Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Testicular Neoplasms [MESH:D013736] (520)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   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)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Hyperandrogenism [MESH:D017588] (98)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Denys-Drash Syndrome [MESH:D030321] (57)  Frasier Syndrome [MESH:D052159] (57)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Hyperandrogenism [MESH:D017588] (98)  Gonadal Dysgenesis [MESH:D006059] (492)   Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Hypogonadism [MESH:D007006] (1123)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Testicular Neoplasms [MESH:D013736] (520)  Cryptorchidism [MESH:D003456] (215)   Carnevale syndrome [MESH:C535586] (45)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Hypoparathyroidism [MESH:D007011] (376)   Barakat syndrome [MESH:C537907] (71)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Pituitary Diseases [MESH:D010900] (1829)   Diabetes Insipidus [MESH:D003919] (302)   Wolfram Syndrome [MESH:D014929] (37)  Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040)  Goiter [MESH:D006042] (359)   Goiter, Nodular [MESH:D006044] (44)   Pendred syndrome [MESH:C536648] (35)  Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Spondyloenchondrodysplasia [MESH:C535782] (71)  Addison Disease [MESH:D000224] (40)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Pemphigoid, Bullous [MESH:D010391] (707)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Aicardi-Goutieres syndrome 5 [MESH:C535608] (22)  Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)   Diabetes Mellitus, Insulin-Dependent, 22 [MESH:C567284] (72)  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)   Hydrops Fetalis [MESH:D015160] (23)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  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)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)  Immunodeficiency without anhidrotic ectodermal dysplasia [MESH:C536289] (56)  WHIM syndrome [MESH:C536697] (148)  CD8 Deficiency, Familial [MESH:C563824] (41)  Neutrophil Immunodeficiency Syndrome [MESH:C564275] (47)  Invasive Pneumococcal Disease, Recurrent Isolated, 2 [MESH:C564468] (56)  Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)  Immunodeficiency due to Defect in CD3-Zeta [MESH:C565712] (19)  Common Variable Immunodeficiency [MESH:D017074] (70)  Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Dysgammaglobulinemia [MESH:D004406] (67)   IgA Deficiency [MESH:D017098] (45)   Immunoglobulin a deficiency 2 [MESH:C536291] (7)  HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Lymphopenia [MESH:D008231] (990)   Wiskott-Aldrich Syndrome [MESH:D014923] (28)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Chediak-Higashi Syndrome [MESH:D002609] (22)  Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Bare lymphocyte syndrome 2 [MESH:C537079] (61)  Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  X-Linked Combined Immunodeficiency Diseases [MESH:D053632] (42)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 [MESH:C567815] (14)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  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, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)  Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Donnai-Barrow syndrome [MESH:C536390] (40)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Gallstones [MESH:D042882] (350)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Fistula [MESH:D005402] (130)   Digestive System Fistula [MESH:D016154] (102)   Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Hernia [MESH:D006547] (2825)   Hernia, Abdominal [MESH:D046449] (208)   Hernia, Ventral [MESH:D006555] (116)   Hernia, Umbilical [MESH:D006554] (115)  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)   Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Nasal Polyps [MESH:D009298] (129)   Asthma, Nasal Polyps, And Aspirin Intolerance [MESH:C565935] (80)  Pathologic Processes [MESH:D010335] (9863)   Gliosis [MESH:D005911] (1419)  Hyperbilirubinemia [MESH:D006932] (1860)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Leukocytosis [MESH:D007964] (978)  Necrosis [MESH:D009336] (4019)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Tachycardia [MESH:D013610] (3339)  Ventricular Fibrillation [MESH:D014693] (624)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial Fibrillation, Familial, 3 [MESH:C563817] (60)  Atrial Fibrillation, Familial, 4 [MESH:C566244] (20)  Long QT Syndrome [MESH:D008133] (691)   Timothy syndrome [MESH:C536962] (44)  Long Qt Syndrome 6 [MESH:C566333] (20)  Long Qt Syndrome 11 [MESH:C567513] (48)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Death [MESH:D003643] (1328)   Fetal Death [MESH:D005313] (464)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Spondyloepimetaphyseal Dysplasia, Pakistani Type [MESH:C567551] (63)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Hematoma [MESH:D006406] (281)   Hematoma, Epidural, Spinal [MESH:D046748] (167)  Hematoma, Subdural [MESH:D006408] (215)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Hematoma, Subdural [MESH:D006408] (212)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  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)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)   Al Awadi syndrome [MESH:C535612] (30)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  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)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Cardiogenic [MESH:D012770] (269)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Cyanosis [MESH:D003490] (288)  Flushing [MESH:D005483] (506)  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)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Obesity, Morbid [MESH:D009767] (515)  Edema [MESH:D004487] (3726)   Hydrops Fetalis [MESH:D015160] (23)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Neurologic Manifestations [MESH:D009461] (8702)   Orthostatic Intolerance [MESH:D054971] (64)  Paresis [MESH:D010291] (419)  Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (984)   Cerebellar Ataxia [MESH:D002524] (289)   Episodic Ataxia, Type 6 [MESH:C567207] (70)  Chorea [MESH:D002819] (189)   Paroxysmal nonkinesigenic dyskinesia [MESH:C537181] (23)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Memory Disorders [MESH:D008569] (3233)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)   Aphasia [MESH:D001037] (219)  Intellectual Disability [MESH:D008607] (1476)   Coffin-Siris syndrome [MESH:C536436] (102)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Spasticity [MESH:D009128] (187)  Pain [MESH:D010146] (3869)   Pain, Intractable [MESH:D010148] (707)  Back Pain [MESH:D001416] (285)   Low Back Pain [MESH:D017116] (244)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5009)   Olfaction Disorders [MESH:D000857] (105)  Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Deafness [MESH:D003638] (593)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Chudley-Mccullough syndrome [MESH:C535459] (45)  Donnai-Barrow syndrome [MESH:C536390] (40)  Thiamine responsive megaloblastic anemia syndrome [MESH:C536510] (39)  Pendred syndrome [MESH:C536648] (35)  Barakat syndrome [MESH:C537907] (71)  Deafness, Autosomal Recessive 12 [MESH:C563327] (46)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Pain, Intractable [MESH:D010148] (707)  Back Pain [MESH:D001416] (285)   Low Back Pain [MESH:D017116] (244)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Nausea [MESH:D009325] (2300)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperventilation [MESH:D006985] (652)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Hypoventilation [MESH:D007040] (359)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Skin Manifestations [MESH:D012877] (1250)   Cafe-au-Lait Spots [MESH:D019080] (186)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Urological Manifestations [MESH:D020924] (3532)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Dermatitis, Occupational [MESH:D009783] (311)  Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Sleep Disorders, Circadian Rhythm [MESH:D020178] (93)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82) 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)  Lead Poisoning [MESH:D007855] (515)  Manganese Poisoning [MESH:D020149] (2214)  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)  Marijuana Abuse [MESH:D002189] (1132)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Tobacco Use Disorder [MESH:D014029] (628)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholic Intoxication [MESH:D000435] (87)  Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   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)  Heat Stress Disorders [MESH:D018882] (226)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (217)   Hematoma, Subdural [MESH:D006408] (212)  Fractures, Bone [MESH:D050723] (597)   Fractures, Closed [MESH:D005596] (194)  Radiation Injuries [MESH:D011832] (2718)   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)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Acyclic [MESH:D006839] (3563)   Alkenes [MESH:D000475] (2079)   Polyenes [MESH:D011090] (1230)   Alkadienes [MESH:D000466] (121)   Chloroprene [MESH:D002737] (2) 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)   Physical Examination [MESH:D010808] (1041)   Body Constitution [MESH:D001824] (450)   Body Weights and Measures [MESH:D001837] (448)   Body Size [MESH:D049628] (439)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Coffin-Siris syndrome [MESH:C536436] (102)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Mental Disorders [MESH:D001523] (2063)   Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Dementia [MESH:D003704] (471)   Frontotemporal Lobar Degeneration [MESH:D057174] (112)   Frontotemporal Dementia [MESH:D057180] (109)   Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Developmental Disabilities [MESH:D002658] (151)   Malpuech facial clefting syndrome [MESH:C535704] (45)  Intellectual Disability [MESH:D008607] (1109)   Coffin-Siris syndrome [MESH:C536436] (102)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Sleep Disorders [MESH:D012893] (148)   Dyssomnias [MESH:D020920] (101)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (84)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82) 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)   5q- syndrome [MESH:C535323] (131)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  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)   5q- syndrome [MESH:C535323] (131)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Physiological Phenomena [MESH:D010829] (788)   Body Constitution [MESH:D001824] (453)   Body Weights and Measures [MESH:D001837] (444)   Body Size [MESH:D049628] (438)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)