Item 18 of 25 (back to results) previous next   Methylnitrosourea D008770               MeSH Unique Identifier: D008770 Scope Notes: A nitrosourea compound with alkylating, carcinogenic, and mutagenic properties. Chemical – Gene Interaction Note 1: Methylnitrosourea results in decreased expression of CCNA2 Note 2: Methylnitrosourea results in decreased expression of CDK1 Click here for more information

Current search: C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140] > Bone Diseases [MESH:D001847] > Bone Diseases, Developmental [MESH:D001848] > Dysostoses [MESH:D004413] > Synostosis [MESH:D013580] > Syndactyly [MESH:D013576] > Rosselli-Gulienetti Syndrome [MESH:C563117] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Cyclin-dependent kinases [HGNC:CDK] (338)   cyclin-dependent kinase 01 [HGNC:CDK1] (151) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  cotreatment (1499)  Decreases (5154)   expression (2187)  reaction (3393)  response to substance (713)  Increases (5571)   alkylation (18)  carbamoylation (4)  reaction (1574)  response to substance (641) 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)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Face [MESH:D005145] (387)   Nose [MESH:D009666] (71)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Spine [MESH:D013131] (258)   VACTERL hydrocephaly [MESH:C536521] (151)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Intestines [MESH:D007422] (271)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Lower Gastrointestinal Tract [MESH:D041741] (254)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Upper Gastrointestinal Tract [MESH:D041742] (236)   Esophagus [MESH:D004947] (200)   VACTERL hydrocephaly [MESH:C536521] (151)  Liver [MESH:D008099] (24)   Meckel Syndrome, Type 4 [MESH:C567003] (20)  Respiratory System [MESH:D012137] (321)   Nose [MESH:D009666] (91)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Trachea [MESH:D014132] (190)   VACTERL hydrocephaly [MESH:C536521] (151)  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   VACTERL hydrocephaly [MESH:C536521] (151)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Nose [MESH:D009666] (74)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Cells [MESH:D002477] (1885)   Blood Cells [MESH:D001773] (196)   Erythrocytes [MESH:D004912] (146)   Erythrocytes, Abnormal [MESH:D004913] (141)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127)  Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  Chromosomes, Human, 16-18 [MESH:D002902] (799)   Chromosomes, Human, Pair 17 [MESH:D002886] (779)   Chromosome 17 deletion [MESH:C538045] (769)  Inclusion Bodies [MESH:D002479] (147)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127)  Hemic and Immune Systems [MESH:D006424] (272)   Blood [MESH:D001769] (200)   Blood Cells [MESH:D001773] (194)   Erythrocytes [MESH:D004912] (146)   Erythrocytes, Abnormal [MESH:D004913] (141)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Enterobacteriaceae Infections [MESH:D004756] (669)   Salmonella Infections [MESH:D012480] (620)   Salmonella Infections, Animal [MESH:D012481] (604)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Tuberculosis [MESH:D014376] (992)   Tuberculosis, Bovine [MESH:D014380] (380)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Urinary Tract Infections [MESH:D014552] (984)  Intraabdominal Infections [MESH:D059413] (958)   Appendicitis [MESH:D001064] (774)  Peritonitis [MESH:D010538] (800)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Papillomavirus Infections [MESH:D030361] (630)  Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Slow Virus Diseases [MESH:D012897] (782)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  Tumor Virus Infections [MESH:D014412] (1069)   Papillomavirus Infections [MESH:D030361] (537)  Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   Nematode Infections [MESH:D009349] (870)   Adenophorea Infections [MESH:D017188] (808)   Enoplida Infections [MESH:D017189] (807)   Trichuriasis [MESH:D014257] (805)  Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Protozoan Infections [MESH:D011528] (3014)   Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Visceral [MESH:D007898] (2149)  Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Malaria [MESH:D008288] (2175)   Malaria, Falciparum [MESH:D016778] (438)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Tuberous Sclerosis [MESH:D014402] (635)  Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Hepatoblastoma [MESH:D018197] (548)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Lipoma [MESH:D008067] (159)  Liposarcoma [MESH:D008080] (612)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Cutaneous [MESH:D034701] (45)  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, Abdominal [MESH:D018221] (56)  Fibromatosis, Aggressive [MESH:D018222] (1562)   Desmoid disease, hereditary [MESH:C535944] (58)  Fibrosarcoma [MESH:D005354] (90)   Neurofibrosarcoma [MESH:D018319] (44)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Liposarcoma [MESH:D008080] (612)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Fibrosarcoma [MESH:D005354] (90)   Neurofibrosarcoma [MESH:D018319] (44)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Germinoma [MESH:D018237] (201)   Seminoma [MESH:D018239] (195)  Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  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)  Neurilemmoma [MESH:D009442] (36)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Ovarian epithelial cancer [MESH:C538090] (57)  Adenoma [MESH:D000236] (4051)   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)   Desmoid disease, hereditary [MESH:C535944] (58)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Adenocarcinoma, Papillary [MESH:D000231] (7)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  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)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Pilomatrixoma [MESH:D018296] (252)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, 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)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  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)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Nerve Sheath Neoplasms [MESH:D018317] (365)   Neurofibrosarcoma [MESH:D018319] (44)  Neurofibroma [MESH:D009455] (177)   Neurofibrosarcoma [MESH:D018319] (44)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Neuroma [MESH:D009463] (37)   Neurilemmoma [MESH:D009442] (36)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  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)  Neurilemmoma [MESH:D009442] (35)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangioma [MESH:D006391] (690)  Hemangiosarcoma [MESH:D006394] (1836)  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)  Nevus [MESH:D009506] (340)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neoplasms by Site [MESH:D009371] (9169)   Soft Tissue Neoplasms [MESH:D012983] (2003)  Abdominal Neoplasms [MESH:D000008] (74)   Desmoid disease, hereditary [MESH:C535944] (58)  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)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  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)   Testicular Neoplasms [MESH:D013736] (520)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Ovarian Neoplasms [MESH:D010051] (3275)   Ovarian epithelial cancer [MESH:C538090] (57)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Eye Neoplasms [MESH:D005134] (400)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  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)   Turcot syndrome [MESH:C536928] (159)  Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Skin Neoplasms [MESH:D012878] (2992)   Sebaceous Gland Neoplasms [MESH:D012626] (154)   Muir-Torre Syndrome [MESH:D055653] (102)  Thoracic Neoplasms [MESH:D013899] (6032)   Thymus Neoplasms [MESH:D013953] (247)  Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Vaginal Neoplasms [MESH:D014625] (363)  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)  Testicular Neoplasms [MESH:D013736] (520)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  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)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Tuberous Sclerosis [MESH:D014402] (635)  Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Turcot syndrome [MESH:C536928] (159)  Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Tuberous Sclerosis [MESH:D014402] (635)  Wilms Tumor [MESH:D009396] (553)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Lynch Syndrome II [MESH:D055847] (103)   Muir-Torre Syndrome [MESH:D055653] (102)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Precancerous Conditions [MESH:D011230] (2858)   Aberrant Crypt Foci [MESH:D058739] (326)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group F [MESH:C562592] (38)  XFE Progeroid Syndrome [MESH:C567043] (38)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Diseases, Developmental [MESH:D001848] (3315)   Proteus Syndrome [MESH:D016715] (152)  Dwarfism [MESH:D004392] (778)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Seckel syndrome 1 [MESH:C537533] (63)  Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Cockayne Syndrome [MESH:D003057] (107)   XFE Progeroid Syndrome [MESH:C567043] (38)  Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Osteochondrodysplasias [MESH:D010009] (2440)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Osteoglophonic dwarfism [MESH:C536050] (90)  Smith-McCort Dysplasia [MESH:C564589] (19)  Fibrous Dysplasia of Bone [MESH:D005357] (737)  Bone Diseases, Endocrine [MESH:D001849] (747)   Acromegaly [MESH:D000172] (466)  Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)  Spinal Diseases [MESH:D013122] (2485)   Spinal Curvatures [MESH:D013121] (742)   Kyphosis [MESH:D007738] (637)  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)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Jackson-Weiss syndrome [MESH:C537559] (149)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Joint Diseases [MESH:D007592] (4657)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Ankylosis [MESH:D000844] (479)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Muscle Weakness [MESH:D018908] (478)  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 Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Costello Syndrome [MESH:D056685] (407)  Craniofacial Dysostosis [MESH:D003394] (391)  Donohue Syndrome [MESH:D056731] (95)  LEOPARD Syndrome [MESH:D044542] (299)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Retrognathia [MESH:D063173] (110)   Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Microcephaly [MESH:D008831] (700)   Seckel syndrome 1 [MESH:C537533] (63)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 4 [MESH:C548082] (37)  Noonan Syndrome 6 [MESH:C548084] (44)  Plagiocephaly [MESH:D059041] (440)   Plagiocephaly, Nonsynostotic [MESH:D049068] (85)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Limb Deformities, Congenital [MESH:D017880] (1813)   VACTERL hydrocephaly [MESH:C536521] (151)  Brachydactyly [MESH:D059327] (220)  Proteus Syndrome [MESH:D016715] (152)  Ectromelia [MESH:D004480] (108)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Jackson-Weiss syndrome [MESH:C537559] (149)  Polydactyly [MESH:D017689] (318)   Meckel Syndrome, Type 4 [MESH:C567003] (20)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  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)  Cholangitis [MESH:D002761] (203)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Hirschsprung Disease [MESH:D006627] (361)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  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)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Stenosis [MESH:D004940] (490)  Esophagitis [MESH:D004941] (1120)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Gastroenteritis [MESH:D005759] (4066)   Appendicitis [MESH:D001064] (774)  Esophagitis [MESH:D004941] (1120)  Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   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)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Appendicitis [MESH:D001064] (774)  Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colonic Diseases, Functional [MESH:D003109] (439)   Irritable Bowel Syndrome [MESH:D043183] (429)  Colorectal Neoplasms [MESH:D015179] (5282)   Turcot syndrome [MESH:C536928] (159)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   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)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Intestinal Polyposis [MESH:D044483] (1610)   Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   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)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   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, Animal [MESH:D006520] (260)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  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)  Peritoneal Diseases [MESH:D010532] (1119)   Peritonitis [MESH:D010538] (800) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  PCI 5002 [MESH:C568608] (527)  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)  Oral Ulcer [MESH:D019226] (488)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  PCI 5002 [MESH:C568608] (433)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  PCI 5002 [MESH:C568608] (433)  Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  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)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Retrognathia [MESH:D063173] (110)   Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (98)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Orofacial Cleft 12 [MESH:C567548] (434)  Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Tooth Agenesis, Selective, 6 [MESH:C567755] (154)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Tooth Agenesis, Selective, 6 [MESH:C567755] (154) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Lung Diseases [MESH:D008171] (7249)   Hypertension, Pulmonary [MESH:D006976] (2000)  Pulmonary Edema [MESH:D011654] (2109)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Alveolitis, Extrinsic Allergic [MESH:D000542] (496)  Idiopathic Interstitial Pneumonias [MESH:D054988] (314)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  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)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Pulmonary Fibrosis [MESH:D011658] (3140)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Insufficiency [MESH:D012131] (841)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Rhinitis [MESH:D012220] (766)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness [MESH:D003638] (623)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Pendred syndrome [MESH:C536648] (35)  Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Griscelli syndrome type 1 [MESH:C537301] (42)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 39 [MESH:C564265] (137)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Chronobiology Disorders [MESH:D021081] (970)  Sleep Disorders [MESH:D012893] (2050)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Wernicke Encephalopathy [MESH:D014899] (75)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Joubert syndrome 5 [MESH:C537688] (20)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  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 Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Lewy Body Disease [MESH:D020961] (1143)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsies, Partial [MESH:D004828] (1267)   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)  Hydrocephalus [MESH:D006849] (276)   VACTERL hydrocephaly [MESH:C536521] (151)  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)   Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Hyperpituitarism [MESH:D006964] (1250)   Acromegaly [MESH:D000172] (466)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Hypopituitarism [MESH:D007018] (732)   Hypopituitarism and septooptic 'dysplasia' [MESH:C531815] (11)  Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)   VACTERL hydrocephaly [MESH:C536521] (151)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Movement Disorders [MESH:D009069] (4823)   Dystonic Disorders [MESH:D020821] (729)   Juvenile-onset dystonia [MESH:C537704] (143)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Ocular Motility Disorders [MESH:D015835] (364)   Joubert syndrome 5 [MESH:C537688] (20)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Joubert syndrome 5 [MESH:C537688] (20)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Malformations of Cortical Development [MESH:D054220] (1406)   Neuronal Migration Disorders [MESH:D054081] (264)  Tuberous Sclerosis [MESH:D014402] (635)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Microcephaly [MESH:D008831] (700)   Seckel syndrome 1 [MESH:C537533] (63)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Meckel Syndrome, Type 4 [MESH:C567003] (20)  Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Septo-Optic Dysplasia [MESH:D025962] (17)   Hypopituitarism and septooptic 'dysplasia' [MESH:C531815] (11)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Peripheral Nervous System Neoplasms [MESH:D010524] (287)   Nerve Sheath Neoplasms [MESH:D018317] (286)   Neurofibroma [MESH:D009455] (47)   Neurofibrosarcoma [MESH:D018319] (44)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Tuberous Sclerosis [MESH:D014402] (635)  von Hippel-Lindau Disease [MESH:D006623] (580)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Alexander Disease [MESH:D038261] (168)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Tuberous Sclerosis [MESH:D014402] (635)  Cockayne Syndrome [MESH:D003057] (107)   XFE Progeroid Syndrome [MESH:C567043] (38)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  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)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Korsakoff Syndrome [MESH:D020915] (69)  Intellectual Disability [MESH:D008607] (3054)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypotonia [MESH:D009123] (258)   Joubert syndrome 5 [MESH:C537688] (20)  Pain [MESH:D010146] (3875)   Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness [MESH:D003638] (623)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Pendred syndrome [MESH:C536648] (35)  Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Griscelli syndrome type 1 [MESH:C537301] (42)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 39 [MESH:C564265] (137)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Diseases [MESH:D009135] (3538)   Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  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)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Neurofibromatosis 1 [MESH:D009456] (117)  Mononeuropathies [MESH:D020422] (604)   Sciatic Neuropathy [MESH:D020426] (477)  Peripheral Nervous System Neoplasms [MESH:D010524] (287)   Nerve Sheath Neoplasms [MESH:D018317] (286)   Neurofibroma [MESH:D009455] (47)   Neurofibrosarcoma [MESH:D018319] (44)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eyelid Diseases [MESH:D005141] (882)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Albinism [MESH:D000417] (258)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Oculocutaneous albinism type 2 [MESH:C537730] (36)  Oculocutaneous albinism type 3 [MESH:C537731] (40)  Leber Congenital Amaurosis [MESH:D057130] (157)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Leber Congenital Amaurosis 10 [MESH:C565720] (20)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Eye Neoplasms [MESH:D005134] (413)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Ocular Motility Disorders [MESH:D015835] (1699)   Joubert syndrome 5 [MESH:C537688] (20)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Refractive Errors [MESH:D012030] (457)   Anisometropia [MESH:D015858] (152)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Leber Congenital Amaurosis [MESH:D057130] (157)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Leber Congenital Amaurosis 10 [MESH:C565720] (20)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Edema [MESH:D008269] (557)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Testicular Neoplasms [MESH:D013736] (520)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)   Follicle-stimulating hormone deficiency, isolated [MESH:C537070] (185)  Penile Diseases [MESH:D010409] (1805)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Diseases [MESH:D011469] (6204)   Prostatitis [MESH:D011472] (424)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  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)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Urogenital Abnormalities [MESH:D014564] (2065)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  Gonadal Dysgenesis [MESH:D006059] (492)   Turner Syndrome [MESH:D014424] (131)  Sex Chromosome Disorders of Sex Development [MESH:D058533] (137)   Turner Syndrome [MESH:D014424] (131)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Testicular Neoplasms [MESH:D013736] (520)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  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)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Joubert syndrome 5 [MESH:C537688] (20)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Polycystic Kidney Diseases [MESH:D007690] (853)   Meckel Syndrome, Type 4 [MESH:C567003] (20)  Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  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)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hematuria [MESH:D006417] (477)   Hematuria, Benign Familial [MESH:C562476] (25)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57)  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 Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Ovarian epithelial cancer [MESH:C538090] (57)  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)  Vaginal Diseases [MESH:D014623] (446)   Vaginal Neoplasms [MESH:D014625] (363)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Abnormalities [MESH:D014564] (2043)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  Gonadal Dysgenesis [MESH:D006059] (492)   Turner Syndrome [MESH:D014424] (131)  Sex Chromosome Disorders of Sex Development [MESH:D058533] (137)   Turner Syndrome [MESH:D014424] (131)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Vaginal Neoplasms [MESH:D014625] (363)  Ovarian Neoplasms [MESH:D010051] (3281)   Ovarian epithelial cancer [MESH:C538090] (57)  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)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Joubert syndrome 5 [MESH:C537688] (20)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Polycystic Kidney Diseases [MESH:D007690] (853)   Meckel Syndrome, Type 4 [MESH:C567003] (20)  Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  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)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Glycosuria [MESH:D006029] (100)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hematuria [MESH:D006417] (477)   Hematuria, Benign Familial [MESH:C562476] (25)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57)  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)   Diabetes, Gestational [MESH:D016640] (1157)  Placenta Diseases [MESH:D010922] (1781)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Abortion, Spontaneous [MESH:D000022] (2780)   Embryo Loss [MESH:D020964] (288)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316)  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)  VACTERL hydrocephaly [MESH:C536521] (151)  LEOPARD Syndrome [MESH:D044542] (299)  Turner Syndrome [MESH:D014424] (131)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 4 [MESH:C548082] (37)  Noonan Syndrome 6 [MESH:C548084] (44)  Heart Diseases [MESH:D006331] (8614)   Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Atrial Fibrillation [MESH:D001281] (1053)  Brugada Syndrome [MESH:D053840] (195)  Heart Block [MESH:D006327] (571)  Long QT Syndrome [MESH:D008133] (693)  Tachycardia [MESH:D013610] (3339)  Ventricular Fibrillation [MESH:D014693] (624)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VACTERL hydrocephaly [MESH:C536521] (151)  LEOPARD Syndrome [MESH:D044542] (299)  Turner Syndrome [MESH:D014424] (131)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 4 [MESH:C548082] (37)  Noonan Syndrome 6 [MESH:C548084] (44)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   LEOPARD Syndrome [MESH:D044542] (299)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Valve, Calcification of [MESH:C562942] (655)  Vascular Diseases [MESH:D014652] (8691)   Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Retinal Vein Occlusion [MESH:D012170] (607)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Coronary Artery Disease [MESH:D003324] (2685)  Atherosclerosis [MESH:D050197] (4188)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  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 Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  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, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  No-Reflow Phenomenon [MESH:D054318] (277)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Methemoglobinemia [MESH:D008708] (850)  Polycythemia [MESH:D011086] (412)  Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Hemolytic [MESH:D000743] (3083)   CD59 Deficiency [MESH:C567355] (57)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Heinz Body Anemias [MESH:C563030] (127)  Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)  beta-Thalassemia [MESH:D017086] (458)  Hemoglobinuria, Paroxysmal [MESH:D006457] (293)   Bone Marrow failure syndromes [MESH:C536572] (248)  Glycosylphosphatidylinositol deficiency [MESH:C537277] (61)  Anemia, Macrocytic [MESH:D000748] (382)   5q- syndrome [MESH:C535323] (131)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  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)   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)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Hemoglobinuria, Paroxysmal [MESH:D006457] (293)   Bone Marrow failure syndromes [MESH:C536572] (248)  Glycosylphosphatidylinositol deficiency [MESH:C537277] (61)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Polycythemia Vera [MESH:D011087] (244)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)  beta-Thalassemia [MESH:D017086] (458)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Leukocyte Disorders [MESH:D007960] (2662)   Leukocytosis [MESH:D007964] (988)  Leukostasis [MESH:D018921] (769)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)  Thrombophilia [MESH:D019851] (592)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Lymphatic Diseases [MESH:D008206] (5167)   Thymus Neoplasms [MESH:D013953] (247)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) 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)  Abnormalities, Multiple [MESH:D000015] (3192)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)  Bardet-Biedl Syndrome [MESH:D020788] (110)  Costello Syndrome [MESH:D056685] (407)  Donohue Syndrome [MESH:D056731] (95)  LEOPARD Syndrome [MESH:D044542] (299)  Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Proteus Syndrome [MESH:D016715] (152)  Cockayne Syndrome [MESH:D003057] (107)   XFE Progeroid Syndrome [MESH:C567043] (38)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Waardenburg Syndrome [MESH:D014849] (243)   ABCD syndrome [MESH:C535334] (143)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VACTERL hydrocephaly [MESH:C536521] (151)  LEOPARD Syndrome [MESH:D044542] (299)  Long QT Syndrome [MESH:D008133] (693)  Turner Syndrome [MESH:D014424] (131)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 4 [MESH:C548082] (37)  Noonan Syndrome 6 [MESH:C548084] (44)  Chromosome Disorders [MESH:D025063] (2030)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Sex Chromosome Disorders [MESH:D025064] (479)   Sex Chromosome Disorders of Sex Development [MESH:D058533] (136)   Turner Syndrome [MESH:D014424] (131)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Craniofacial Dysostosis [MESH:D003394] (391)  LEOPARD Syndrome [MESH:D044542] (299)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Microcephaly [MESH:D008831] (700)   Seckel syndrome 1 [MESH:C537533] (63)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 4 [MESH:C548082] (37)  Noonan Syndrome 6 [MESH:C548084] (44)  Plagiocephaly [MESH:D059041] (440)   Plagiocephaly, Nonsynostotic [MESH:D049068] (85)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Limb Deformities, Congenital [MESH:D017880] (1813)   VACTERL hydrocephaly [MESH:C536521] (151)  Brachydactyly [MESH:D059327] (220)  Lower Extremity Deformities, Congenital [MESH:D038061] (81)  Proteus Syndrome [MESH:D016715] (152)  Ectromelia [MESH:D004480] (108)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Foot Deformities, Congenital [MESH:D005532] (538)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Jackson-Weiss syndrome [MESH:C537559] (149)  Hand Deformities, Congenital [MESH:D006228] (587)   Laurin-Sandrow syndrome [MESH:C535689] (15)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Polydactyly [MESH:D017689] (318)   Meckel Syndrome, Type 4 [MESH:C567003] (20)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Malformations of Cortical Development [MESH:D054220] (1406)   Neuronal Migration Disorders [MESH:D054081] (264)  Tuberous Sclerosis [MESH:D014402] (635)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Microcephaly [MESH:D008831] (700)   Seckel syndrome 1 [MESH:C537533] (63)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Meckel Syndrome, Type 4 [MESH:C567003] (20)  Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Septo-Optic Dysplasia [MESH:D025962] (17)   Hypopituitarism and septooptic 'dysplasia' [MESH:C531815] (11)  Skin Abnormalities [MESH:D012868] (1723)   Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Dyskeratosis Congenita [MESH:D019871] (185)   Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group F [MESH:C562592] (38)  XFE Progeroid Syndrome [MESH:C567043] (38)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Retrognathia [MESH:D063173] (110)   Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Cleft Palate [MESH:D002972] (1330)   Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Tooth Abnormalities [MESH:D014071] (622)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Urogenital Abnormalities [MESH:D014564] (2064)   Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  Gonadal Dysgenesis [MESH:D006059] (492)   Turner Syndrome [MESH:D014424] (131)  Sex Chromosome Disorders of Sex Development [MESH:D058533] (137)   Turner Syndrome [MESH:D014424] (131)  Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Brugada Syndrome [MESH:D053840] (195)  Costello Syndrome [MESH:D056685] (407)  Donohue Syndrome [MESH:D056731] (95)  Kallmann Syndrome [MESH:D017436] (147)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Heinz Body Anemias [MESH:C563030] (127)  Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)  beta-Thalassemia [MESH:D017086] (458)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Chromosome Disorders [MESH:D025063] (2030)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Sex Chromosome Disorders [MESH:D025064] (479)   Sex Chromosome Disorders of Sex Development [MESH:D058533] (136)   Turner Syndrome [MESH:D014424] (131)  Dwarfism [MESH:D004392] (783)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Seckel syndrome 1 [MESH:C537533] (63)  Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Cockayne Syndrome [MESH:D003057] (107)   XFE Progeroid Syndrome [MESH:C567043] (38)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Oculocutaneous albinism type 2 [MESH:C537730] (36)  Oculocutaneous albinism type 3 [MESH:C537731] (40)  Piebaldism [MESH:D016116] (167)   Griscelli syndrome type 1 [MESH:C537301] (42)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Dyskeratosis Congenita [MESH:D019871] (185)   Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)  beta-Thalassemia [MESH:D017086] (458)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Alexander Disease [MESH:D038261] (168)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Tuberous Sclerosis [MESH:D014402] (635)  Cockayne Syndrome [MESH:D003057] (107)   XFE Progeroid Syndrome [MESH:C567043] (38)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Senior-Loken Syndrome 6 [MESH:C565708] (20)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Oculocutaneous albinism type 2 [MESH:C537730] (36)  Oculocutaneous albinism type 3 [MESH:C537731] (40)  Piebaldism [MESH:D016116] (167)   Griscelli syndrome type 1 [MESH:C537301] (42)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   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)   Hemochromatosis [MESH:D006432] (1694)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Turcot syndrome [MESH:C536928] (159)  Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Tuberous Sclerosis [MESH:D014402] (635)  Wilms Tumor [MESH:D009396] (553)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Lynch Syndrome II [MESH:D055847] (103)   Muir-Torre Syndrome [MESH:D055653] (102)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Oculocutaneous albinism type 2 [MESH:C537730] (36)  Oculocutaneous albinism type 3 [MESH:C537731] (40)  Piebaldism [MESH:D016116] (167)   Griscelli syndrome type 1 [MESH:C537301] (42)  Dyskeratosis Congenita [MESH:D019871] (185)   Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group F [MESH:C562592] (38)  XFE Progeroid Syndrome [MESH:C567043] (38)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Collagen Diseases [MESH:D003095] (1267)   Nephritis, Hereditary [MESH:D009394] (62)   Alport syndrome, recessive type [MESH:C536587] (35)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Noonan Syndrome 4 [MESH:C548082] (37)  Noonan Syndrome 6 [MESH:C548084] (44)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Keratosis [MESH:D007642] (1941)  Lipomatosis [MESH:D008068] (182)  Scleroderma, Localized [MESH:D012594] (1597)  Scleroderma, Systemic [MESH:D012595] (199)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hypotrichosis [MESH:D007039] (1513)   Hypotrichosis simplex [MESH:C537160] (92)  Alopecia [MESH:D000505] (1453)  Mastocytosis [MESH:D008415] (60)   Mastocytosis, Cutaneous [MESH:D034701] (45)  Photosensitivity Disorders [MESH:D010787] (272)   Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group F [MESH:C562592] (38)  XFE Progeroid Syndrome [MESH:C567043] (38)  Pigmentation Disorders [MESH:D010859] (1215)   Griscelli syndrome type 1 [MESH:C537301] (42)  Cafe-au-Lait Spots [MESH:D019080] (186)   Cafe au lait spots, multiple [MESH:C537421] (102)  Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Acanthosis Nigricans [MESH:D000052] (203)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)  Hypopigmentation [MESH:D017496] (718)   Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Oculocutaneous albinism type 2 [MESH:C537730] (36)  Oculocutaneous albinism type 3 [MESH:C537731] (40)  Piebaldism [MESH:D016116] (167)   Griscelli syndrome type 1 [MESH:C537301] (42)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group F [MESH:C562592] (38)  XFE Progeroid Syndrome [MESH:C567043] (38)  Scalp Dermatoses [MESH:D012536] (99)   Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Sebaceous Gland Diseases [MESH:D012625] (245)   Sebaceous Gland Neoplasms [MESH:D012626] (154)   Muir-Torre Syndrome [MESH:D055653] (102)  Skin Abnormalities [MESH:D012868] (1709)   Cutis Gyrata Syndrome of Beare And Stevenson [MESH:C565129] (85)  Dyskeratosis Congenita [MESH:D019871] (185)   Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group F [MESH:C562592] (38)  XFE Progeroid Syndrome [MESH:C567043] (38)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Dermatitis, Atopic [MESH:D003876] (2052)  Muir-Torre Syndrome [MESH:D055653] (102)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Oculocutaneous albinism type 2 [MESH:C537730] (36)  Oculocutaneous albinism type 3 [MESH:C537731] (40)  Piebaldism [MESH:D016116] (167)   Griscelli syndrome type 1 [MESH:C537301] (42)  Dyskeratosis Congenita [MESH:D019871] (185)   Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Rosselli-Gulienetti Syndrome [MESH:C563117] (25)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group F [MESH:C562592] (38)  XFE Progeroid Syndrome [MESH:C567043] (38)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Skin Neoplasms [MESH:D012878] (2991)   Sebaceous Gland Neoplasms [MESH:D012626] (154)   Muir-Torre Syndrome [MESH:D055653] (102) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Z. Exceptions (817)   Not Fully Specified [NFS] (817)  Metabolic Diseases [MESH:D008659] (9025)   Metabolic Syndrome X [MESH:D024821] (2151)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Wernicke Encephalopathy [MESH:D014899] (75)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Fanconi Anemia [MESH:D005199] (1604)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Cockayne Syndrome [MESH:D003057] (107)   XFE Progeroid Syndrome [MESH:C567043] (38)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group F [MESH:C562592] (38)  XFE Progeroid Syndrome [MESH:C567043] (38)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes, Gestational [MESH:D016640] (1152)  Donohue Syndrome [MESH:D056731] (95)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction [MESH:C565225] (56)  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)   Hyperinsulinemic Hypoglycemia, Familial, 5 [MESH:C566494] (94)  Insulin Resistance [MESH:D007333] (3511)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   Hyperinsulinemic Hypoglycemia, Familial, 5 [MESH:C566494] (94)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipomatosis [MESH:D008068] (182)  Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)  Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Oculocutaneous albinism type 2 [MESH:C537730] (36)  Oculocutaneous albinism type 3 [MESH:C537731] (40)  Piebaldism [MESH:D016116] (167)   Griscelli syndrome type 1 [MESH:C537301] (42)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   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)   Hemochromatosis [MESH:D006432] (1694)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Lesch-Nyhan Syndrome [MESH:D007926] (129)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Glycosuria, Renal [MESH:D006030] (50)   Cataract, Juvenile, With Microcornea And Glucosuria [MESH:C567434] (26)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Mitochondrial Diseases [MESH:D028361] (2561)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  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)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Proteostasis Deficiencies [MESH:D057165] (3522)   TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hyponatremia [MESH:D007010] (789)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)   Keratomalacia [MESH:C536156] (61)  Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Thiamine Deficiency [MESH:D013832] (139)   Wernicke Encephalopathy [MESH:D014899] (75)  Vitamin D Deficiency [MESH:D014808] (360)   Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Obesity, Morbid [MESH:D009767] (515)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Donohue Syndrome [MESH:D056731] (95)  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 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction [MESH:C565225] (56)  Dwarfism [MESH:D004392] (698)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Seckel syndrome 1 [MESH:C537533] (63)  Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Testicular Neoplasms [MESH:D013736] (520)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Ovarian Neoplasms [MESH:D010051] (3275)   Ovarian epithelial cancer [MESH:C538090] (57)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  Gonadal Dysgenesis [MESH:D006059] (492)   Turner Syndrome [MESH:D014424] (131)  Sex Chromosome Disorders of Sex Development [MESH:D058533] (137)   Turner Syndrome [MESH:D014424] (131)  Hypogonadism [MESH:D007006] (1123)   Kallmann Syndrome [MESH:D017436] (147)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Ovarian epithelial cancer [MESH:C538090] (57)  Testicular Diseases [MESH:D013733] (777)   Testicular Neoplasms [MESH:D013736] (520)  Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)  Pituitary Diseases [MESH:D010900] (1829)   Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Hypopituitarism [MESH:D007018] (732)   Hypopituitarism and septooptic 'dysplasia' [MESH:C531815] (11)  Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Goiter, Nodular [MESH:D006044] (44)   Pendred syndrome [MESH:C536648] (35)  Hyperthyroidism [MESH:D006980] (1191)   Thyroid Hormone Resistance, Selective Pituitary [MESH:C564154] (113)  Hyperthyroxinemia [MESH:D006981] (659)   Thyroid Hormone Resistance Syndrome [MESH:D018382] (135)   Thyroid Hormone Resistance, Generalized, Autosomal Dominant [MESH:C567934] (113)  Thyroid Hormone Resistance, Generalized, Autosomal Recessive [MESH:C567936] (113)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Urticaria [MESH:D014581] (2668)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Lymphopenia [MESH:D008231] (990)  HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Hepatitis, Animal [MESH:D006520] (260)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Salmonella Infections, Animal [MESH:D012481] (604)  Cattle Diseases [MESH:D002418] (416)   Tuberculosis, Bovine [MESH:D014380] (380) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Plaque, Atherosclerotic [MESH:D058226] (696)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Hernia [MESH:D006547] (2825)   Encephalocele [MESH:D004677] (151)   Meckel Syndrome, Type 4 [MESH:C567003] (20)  Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Hypertrophy [MESH:D006984] (4476)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Hepatomegaly [MESH:D006529] (1169)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Azotemia [MESH:D053099] (326)  Emphysema [MESH:D004646] (1096)  Fibrosis [MESH:D005355] (3133)  Gliosis [MESH:D005911] (1419)  Hyperbilirubinemia [MESH:D006932] (1860)  Hyperplasia [MESH:D006965] (2463)  Leukocytosis [MESH:D007964] (978)  Muscle Weakness [MESH:D018908] (478)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Heart Block [MESH:D006327] (571)  Long QT Syndrome [MESH:D008133] (691)  Tachycardia [MESH:D013610] (3339)  Ventricular Fibrillation [MESH:D014693] (624)  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)  Chromosome 17 deletion [MESH:C538045] (769)  Death [MESH:D003643] (1328)   Embryo Loss [MESH:D020964] (288)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Macrocephaly Autism Syndrome [MESH:C565342] (151)  Granuloma [MESH:D006099] (587)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Growth Disorders [MESH:D006130] (2438)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Shock, Hemorrhagic [MESH:D012771] (2042)  Hematuria [MESH:D006417] (477)   Hematuria, Benign Familial [MESH:C562476] (25)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  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)  Ischemia [MESH:D007511] (3049)   No-Reflow Phenomenon [MESH:D054318] (277)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  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, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Asthenia [MESH:D001247] (376)  Chills [MESH:D023341] (644)  Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Feminization [MESH:D005262] (655)  Reticulocytosis [MESH:D045262] (514)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)   Obesity, Morbid [MESH:D009767] (515)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Korsakoff Syndrome [MESH:D020915] (69)  Intellectual Disability [MESH:D008607] (1476)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypotonia [MESH:D009123] (258)   Joubert syndrome 5 [MESH:C537688] (20)  Pain [MESH:D010146] (3869)   Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Lacrimoauriculodentodigital syndrome [MESH:C538132] (149)  Deafness [MESH:D003638] (593)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Pendred syndrome [MESH:C536648] (35)  Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Griscelli syndrome type 1 [MESH:C537301] (42)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 39 [MESH:C564265] (137)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Neuralgia [MESH:D009437] (2074)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Respiratory Sounds [MESH:D012135] (713)  Skin Manifestations [MESH:D012877] (1250)   Cafe-au-Lait Spots [MESH:D019080] (186)   Cafe au lait spots, multiple [MESH:C537421] (102)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Manganese Poisoning [MESH:D020149] (2214)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Wernicke Encephalopathy [MESH:D014899] (75)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69)  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) 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)  Vascular System Injuries [MESH:D057772] (2086)  Wounds, Penetrating [MESH:D014950] (146)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Nitroso Compounds [MESH:D009603] (680)   Nitrosourea Compounds [MESH:D009607] (267)   Methylnitrosourea [MESH:D008770] (18)  Urea [MESH:D014508] (1322)   Nitrosourea Compounds [MESH:D009607] (267)   Methylnitrosourea [MESH:D008770] (18) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Diagnostic Imaging [MESH:D003952] (623)   Ultrasonography [MESH:D014463] (482)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Diagnostic Techniques, Cardiovascular [MESH:D003935] (521)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Physical Examination [MESH:D010808] (1041)   Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Macrocephaly Autism Syndrome [MESH:C565342] (151) 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)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Child Development Disorders, Pervasive [MESH:D002659] (157)   Autistic Disorder [MESH:D001321] (154)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Intellectual Disability [MESH:D008607] (1109)   Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)  Zlotogora-Ogur syndrome [MESH:C536726] (25)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Scaphocephaly, Maxillary Retrusion, And Mental Retardation [MESH:C566511] (85) 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)  Chromosome 17 deletion [MESH:C538045] (769)  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)  Chromosomes, Human, 16-18 [MESH:D002902] (799)   Chromosomes, Human, Pair 17 [MESH:D002886] (779)   Chromosome 17 deletion [MESH:C538045] (769)  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 17 deletion [MESH:C538045] (769)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Chromosome 17 deletion [MESH:C538045] (769)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Chromosome 17 deletion [MESH:C538045] (769)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Chromosome 17 deletion [MESH:C538045] (769)  Physiological Phenomena [MESH:D010829] (788)   Pharmacological Phenomena [MESH:D002620] (173)   Drug Resistance [MESH:D004351] (139)   Insulin Resistance [MESH:D007333] (97)   Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans [MESH:C562710] (94)  Circulatory and Respiratory Physiological Phenomena [MESH:D002943] (614)   Cardiovascular Physiological Phenomena [MESH:D002320] (525)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)