Item 3 of 143 (back to results) previous next   bis(tri-n-butyltin)oxide C005961               MeSH Unique Identifier: C005961 Chemical – Gene Interaction Note 1: Bis(tri-n-butyltin)oxide affects the localization of ATF3 protein Note 2: Bis(tri-n-butyltin)oxide results in increased expression of ATF3 mRNA Click here for more information

Current search: C04. Neoplasms: Neoplasms [MESH:D009369] > Neoplastic Syndromes, Hereditary [MESH:D009386] > Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Basic leucine zipper proteins [HGNC:bZIP] (670)   X-box binding protein 1 [HGNC:XBP1] (79)  BTB domain containing [HGNC:BTBD] (83)   kelch-like ECH-associated protein 1 [HGNC:KEAP1] (50)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566)  cytochrome P450, family 01, subfamily A, polypeptide 02 [HGNC:CYP1A2] (466)  Glutathione S-transferases [HGNC:GST] (460)   Glutathione S-transferases, soluble [HGNC:SGST] (447)   glutathione S-transferase theta 2 [HGNC:GSTT2] (18)  Kelch-like [HGNC:KLHL] (73)   kelch-like ECH-associated protein 1 [HGNC:KEAP1] (50)  Nuclear hormone receptors [HGNC:NR] (1322)   nuclear receptor subfamily 4, group A, member 1 [HGNC:NR4A1] (68) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   localization (731)  Decreases (5154)   activity (2549)  expression (2187)  Increases (5571)   cleavage (666)  expression (3238)  phosphorylation (1060) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Meier-Gorlin syndrome [MESH:C538012] (133)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Leg Bones [MESH:D007867] (228)   Patella [MESH:D010329] (168)   Meier-Gorlin syndrome [MESH:C538012] (133)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Upper Gastrointestinal Tract [MESH:D041742] (236)   Stomach [MESH:D013270] (49)   Pylorus [MESH:D011708] (36)   Epidermolysis Bullosa Simplex With Pyloric Atresia [MESH:C567408] (34)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Atria [MESH:D006325] (65)   Atrial myxoma, familial [MESH:C538262] (34)  Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Meier-Gorlin syndrome [MESH:C538012] (133)  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Helicobacter Infections [MESH:D016481] (579)  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)   Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Tuberculosis [MESH:D014376] (992)   Tuberculosis, Bovine [MESH:D014380] (380)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Sepsis [MESH:D018805] (3556)  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)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Skin Diseases, Infectious [MESH:D012874] (415)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)   Candidiasis familial chronic mucocutaneous, autosomal recessive [MESH:C537979] (36)  Mycoses [MESH:D009181] (385)   Candidiasis [MESH:D002177] (307)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)   Candidiasis familial chronic mucocutaneous, autosomal recessive [MESH:C537979] (36)  Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)   Candidiasis familial chronic mucocutaneous, autosomal recessive [MESH:C537979] (36) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)  Herpesviridae Infections [MESH:D006566] (1944)   Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)  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)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  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)  Slow Virus Diseases [MESH:D012897] (782)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   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)   Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Pancreatic Cyst [MESH:D010181] (18)   Renal hepatic pancreatic dysplasia Dandy Walker cyst [MESH:C537756] (11)  Hamartoma [MESH:D006222] (1484)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Megakaryoblastic, Acute [MESH:D007947] (279)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphatic Vessel Tumors [MESH:D018190] (171)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Neoplasms, Adipose Tissue [MESH:D018205] (677)   Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Myxoma [MESH:D009232] (78)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Embryonal [MESH:D018233] (98)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Embryonal [MESH:D018233] (98)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Adenoma, Liver Cell [MESH:D018248] (685)  Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Thyroid cancer, papillary [MESH:C536915] (111)  Carcinoma, Lewis Lung [MESH:D018827] (248)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  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)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5358)   Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   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)   Pituitary Neoplasms [MESH:D010911] (981)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Heart Neoplasms [MESH:D006338] (47)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   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)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Carcinoma, Lewis Lung [MESH:D018827] (248)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Tuberous Sclerosis [MESH:D014402] (635)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Tuberous Sclerosis [MESH:D014402] (635)  Peutz-Jeghers Syndrome [MESH:D010580] (51)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Diseases, Developmental [MESH:D001848] (3315)   Weill-Marchesani Syndrome [MESH:D056846] (65)  Dwarfism [MESH:D004392] (778)   Weill-Marchesani Syndrome [MESH:D056846] (65)  Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Osteochondrodysplasias [MESH:D010009] (2440)   Epiphyseal dysplasia, multiple, 3 [MESH:C535503] (9)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)   Intervertebral disc disease [MESH:C535531] (514)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Ossification of Posterior Longitudinal Ligament [MESH:D017887] (99)   Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98)  Cartilage Diseases [MESH:D002357] (438)   Keutel syndrome [MESH:C536167] (102)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Arthrogryposis [MESH:D001176] (329)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Contracture [MESH:D003286] (296)   Bethlem myopathy [MESH:C535436] (108)  Stiff Skin Syndrome [MESH:C566112] (62)  Muscular Diseases [MESH:D009135] (4071)   Dimauro disease [MESH:C536176] (33)  Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)  Compartment Syndromes [MESH:D003161] (80)  Muscle Rigidity [MESH:D009127] (617)  Arthrogryposis [MESH:D001176] (329)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Contracture [MESH:D003286] (303)   Bethlem myopathy [MESH:C535436] (108)  Stiff Skin Syndrome [MESH:C566112] (62)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Bethlem myopathy [MESH:C535436] (108)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Epidermolysa bullosa simplex and limb girdle muscular dystrophy [MESH:C535955] (34)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 3 [MESH:C538350] (70)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Arthrogryposis [MESH:D001176] (329)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Craniofacial Abnormalities [MESH:D019465] (3098)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Limb Deformities, Congenital [MESH:D017880] (1813)   Arachnodactyly [MESH:D054119] (126)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  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)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   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)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Gastroenteritis [MESH:D005759] (4066)   Appendicitis [MESH:D001064] (774)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  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)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Appendicitis [MESH:D001064] (774)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  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)   Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Peutz-Jeghers Syndrome [MESH:D010580] (51)  Malabsorption Syndromes [MESH:D008286] (492)   Celiac Disease [MESH:D002446] (340)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatic Cyst [MESH:D010181] (18)   Renal hepatic pancreatic dysplasia Dandy Walker cyst [MESH:C537756] (11)  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)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Mouth Diseases [MESH:D009059] (4783)   Oral Submucous Fibrosis [MESH:D009914] (2432)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Pneumonia [MESH:D011014] (3482)  Pulmonary Fibrosis [MESH:D011658] (3140)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Berylliosis [MESH:D001607] (2005)  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)   Berylliosis [MESH:D001607] (2005)  Lung Neoplasms [MESH:D008175] (6012)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Nose Diseases [MESH:D009668] (1504)   Nasal Obstruction [MESH:D015508] (132)  Paranasal Sinus Diseases [MESH:D010254] (476)   Sinusitis [MESH:D012852] (469)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Insufficiency [MESH:D012131] (841)   Airway Obstruction [MESH:D000402] (191)   Nasal Obstruction [MESH:D015508] (132)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Sinusitis [MESH:D012852] (469)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   MYH9-Related Disorders [MESH:C535507] (46)  Macrothrombocytopenia progressive deafness [MESH:C537831] (46)  Barakat syndrome [MESH:C537907] (71)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Nose Diseases [MESH:D009668] (1504)   Nasal Obstruction [MESH:D015508] (132)  Paranasal Sinus Diseases [MESH:D010254] (476)   Sinusitis [MESH:D012852] (469)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Chronobiology Disorders [MESH:D021081] (970)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease, Secondary [MESH:D010302] (327)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 7, Autosomal Recessive Early-Onset [MESH:C565238] (62)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Mitochondrial Encephalomyopathies [MESH:D017237] (158)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Leigh Disease [MESH:D007888] (206)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Dandy-Walker Syndrome [MESH:D003616] (50)   Renal hepatic pancreatic dysplasia Dandy Walker cyst [MESH:C537756] (11)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  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)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Hydrocephalus [MESH:D006849] (276)   Dandy-Walker Syndrome [MESH:D003616] (50)   Renal hepatic pancreatic dysplasia Dandy Walker cyst [MESH:C537756] (11)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1250)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)   Dandy-Walker Syndrome [MESH:D003616] (50)   Renal hepatic pancreatic dysplasia Dandy Walker cyst [MESH:C537756] (11)  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)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Central Nervous System Infections [MESH:D002494] (1823)   Prion Diseases [MESH:D017096] (488)   Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Dystonic Disorders [MESH:D020821] (729)   Dystonia, Dopa-responsive [MESH:C538007] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease, Secondary [MESH:D010302] (327)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 7, Autosomal Recessive Early-Onset [MESH:C565238] (62)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Cranial Nerve Diseases [MESH:D003389] (2004)   Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Multiple Sclerosis [MESH:D009103] (1716)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Dandy-Walker Syndrome [MESH:D003616] (50)   Renal hepatic pancreatic dysplasia Dandy Walker cyst [MESH:C537756] (11)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth Disease, Dominant Intermediate B [MESH:C564703] (27)  Malformations of Cortical Development [MESH:D054220] (1406)   Tuberous Sclerosis [MESH:D014402] (635)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Knobloch syndrome [MESH:C537209] (70)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Tuberous Sclerosis [MESH:D014402] (635)  Neurodegenerative Diseases [MESH:D019636] (6613)   Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62)  Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Tuberous Sclerosis [MESH:D014402] (635)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth Disease, Dominant Intermediate B [MESH:C564703] (27)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 7, Autosomal Recessive Early-Onset [MESH:C565238] (62)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Prion Diseases [MESH:D017096] (475)   Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neurologic Manifestations [MESH:D009461] (8964)   Gait Disorders, Neurologic [MESH:D020233] (491)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Sensation Disorders [MESH:D012678] (5011)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   MYH9-Related Disorders [MESH:C535507] (46)  Macrothrombocytopenia progressive deafness [MESH:C537831] (46)  Barakat syndrome [MESH:C537907] (71)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (501)   Blindness [MESH:D001766] (252)  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 Atrophy, Spinal [MESH:D009134] (850)   Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62)  Muscular Diseases [MESH:D009135] (3538)   Dimauro disease [MESH:C536176] (33)  Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Bethlem myopathy [MESH:C535436] (108)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Epidermolysa bullosa simplex and limb girdle muscular dystrophy [MESH:C535955] (34)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 3 [MESH:C538350] (70)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Brachial Plexus Neuropathies [MESH:D020516] (37)   Brachial Plexus Neuritis [MESH:D020968] (31)  Neuritis [MESH:D009443] (55)   Brachial Plexus Neuritis [MESH:D020968] (31)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth Disease, Dominant Intermediate B [MESH:C564703] (27)  Polyradiculoneuropathy [MESH:D011129] (213)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  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)  Ocular Hypertension [MESH:D009798] (1630)  Conjunctival Diseases [MESH:D003229] (273)   Pemphigoid, Benign Mucous Membrane [MESH:D010390] (61)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)  Fuchs' Endothelial Dystrophy [MESH:D005642] (86)   Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)  Ectopia Lentis [MESH:D004479] (73)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Choroideremia [MESH:D015794] (18)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)  Fuchs' Endothelial Dystrophy [MESH:D005642] (86)   Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)  Leber Congenital Amaurosis [MESH:D057130] (157)   Amaurosis congenita of Leber, type 2 [MESH:C536601] (25)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Retinitis Pigmentosa 18 [MESH:C563320] (17)  Lens Diseases [MESH:D007905] (900)   Lens Subluxation [MESH:D007906] (74)   Ectopia Lentis [MESH:D004479] (73)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Refractive Errors [MESH:D012030] (457)   Myopia [MESH:D009216] (349)   MASS syndrome [MESH:C536030] (62)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Vein Occlusion [MESH:D012170] (607)  Leber Congenital Amaurosis [MESH:D057130] (157)   Amaurosis congenita of Leber, type 2 [MESH:C536601] (25)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Macular Edema [MESH:D008269] (557)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Retinitis Pigmentosa 18 [MESH:C563320] (17)  Retinal Detachment [MESH:D012163] (1639)   Knobloch syndrome [MESH:C537209] (70)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  Choroideremia [MESH:D015794] (18)  Vision Disorders [MESH:D014786] (534)   Blindness [MESH:D001766] (259) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Testicular Diseases [MESH:D013733] (451)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Hyperplasia [MESH:D011470] (336)  Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Urogenital Abnormalities [MESH:D014564] (2065)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Hypospadias [MESH:D007021] (798)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Dimauro disease [MESH:C536176] (33)  Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)  Uremia [MESH:D014511] (2898)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Nephronophthisis 3 [MESH:C565780] (11)  Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrosis [MESH:D009401] (2228)   Barakat syndrome [MESH:C537907] (71)  Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Fanconi Syndrome [MESH:D005198] (253)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  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)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Uterine Diseases [MESH:D014591] (2479)   Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Vaginal Diseases [MESH:D014623] (446)   Vaginal Neoplasms [MESH:D014625] (363)  Urogenital Abnormalities [MESH:D014564] (2043)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Hypospadias [MESH:D007021] (798)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Vaginal Neoplasms [MESH:D014625] (363)  Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Dimauro disease [MESH:C536176] (33)  Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)  Uremia [MESH:D014511] (2898)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Nephronophthisis 3 [MESH:C565780] (11)  Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrosis [MESH:D009401] (2228)   Barakat syndrome [MESH:C537907] (71)  Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Fanconi Syndrome [MESH:D005198] (253)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435) 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)   Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  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)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1i [MESH:C565752] (62)  Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)  Cardiomyopathies [MESH:D009202] (5331)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1i [MESH:C565752] (62)  Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Heart Defects, Congenital [MESH:D006330] (2443)   Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Heart Neoplasms [MESH:D006338] (47)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Heart Valve Prolapse [MESH:D016127] (99)   Mitral Valve Prolapse [MESH:D008945] (96)   MASS syndrome [MESH:C536030] (62)  Pulmonary Valve Stenosis [MESH:D011666] (360)   Keutel syndrome [MESH:C536167] (102)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  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)  Pulmonary Valve Stenosis [MESH:D011666] (109)   Keutel syndrome [MESH:C536167] (102)  Vascular Diseases [MESH:D014652] (8691)   Arteritis [MESH:D001167] (1084)  Compartment Syndromes [MESH:D003161] (80)  Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Peripheral Vascular Diseases [MESH:D016491] (1412)  Retinal Vein Occlusion [MESH:D012170] (607)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Type III [MESH:D056828] (32)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  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)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Thrombosis [MESH:D013927] (3101)   Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypertension [MESH:D006973] (5655)   Hypertension, Renal [MESH:D006977] (698)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Z. Exceptions (453)   Not Fully Specified [NFS] (453)  Hematologic Diseases [MESH:D006402] (6174)   Methemoglobinemia [MESH:D008708] (850)  Anemia [MESH:D000740] (3966)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 9 [MESH:C567650] (43)  Anemia, Hemolytic [MESH:D000743] (3083)   Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Anemia, Macrocytic [MESH:D000748] (382)   5q- syndrome [MESH:C535323] (131)  Red-Cell Aplasia, Pure [MESH:D012010] (183)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 9 [MESH:C567650] (43)  Blood Coagulation Disorders [MESH:D001778] (1828)   Prekallikrein Deficiency [MESH:C562725] (42)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Activated Protein C Resistance [MESH:D020016] (140)  Factor XII Deficiency [MESH:D005175] (31)  Coagulation Protein Disorders [MESH:D020147] (580)   Activated Protein C Resistance [MESH:D020016] (140)  Factor XII Deficiency [MESH:D005175] (31)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   MYH9-Related Disorders [MESH:C535507] (46)  Macrothrombocytopenia progressive deafness [MESH:C537831] (46)  Thrombotic Microangiopathies [MESH:D057049] (2598)  Blood Protein Disorders [MESH:D001796] (3051)   Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)  Myelodysplastic Syndromes [MESH:D009190] (2093)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 9 [MESH:C567650] (43)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Primary Myelofibrosis [MESH:D055728] (165)  Hemorrhagic Disorders [MESH:D006474] (3359)   Factor XII Deficiency [MESH:D005175] (31)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Leukocyte Disorders [MESH:D007960] (2662)   Eosinophilia [MESH:D004802] (537)  Leukopenia [MESH:D007970] (1921)  Leukostasis [MESH:D018921] (769)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)  Polycythemia [MESH:D011086] (412)   Polycythemia, primary familial and congenital [MESH:C536842] (45)  Thrombophilia [MESH:D019851] (592)   Activated Protein C Resistance [MESH:D020016] (140)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphoproliferative Disorders [MESH:D008232] (4638)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  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)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Splenic Diseases [MESH:D013158] (1323)   Hypersplenism [MESH:D006971] (341) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Multiple [MESH:D000015] (3192)   Keutel syndrome [MESH:C536167] (102)  Renal hepatic pancreatic dysplasia Dandy Walker cyst [MESH:C537756] (11)  Bloom Syndrome [MESH:D001816] (107)  Carney Complex [MESH:D056733] (45)  Down Syndrome [MESH:D004314] (1287)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Ectodermal Dysplasia [MESH:D004476] (938)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Chromosome Disorders [MESH:D025063] (2030)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Down Syndrome [MESH:D004314] (1287)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)  Ectopia Lentis [MESH:D004479] (73)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Arthrogryposis [MESH:D001176] (329)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Craniofacial Abnormalities [MESH:D019465] (3064)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Limb Deformities, Congenital [MESH:D017880] (1813)   Arachnodactyly [MESH:D054119] (126)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Dandy-Walker Syndrome [MESH:D003616] (50)   Renal hepatic pancreatic dysplasia Dandy Walker cyst [MESH:C537756] (11)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth Disease, Dominant Intermediate B [MESH:C564703] (27)  Malformations of Cortical Development [MESH:D054220] (1406)   Tuberous Sclerosis [MESH:D014402] (635)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Knobloch syndrome [MESH:C537209] (70)  Skin Abnormalities [MESH:D012868] (1723)   Carney Complex [MESH:D056733] (45)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysa bullosa simplex and limb girdle muscular dystrophy [MESH:C535955] (34)  Epidermolysis bullosa simplex, Ogna type [MESH:C535962] (34)  Epidermolysis Bullosa Simplex With Pyloric Atresia [MESH:C567408] (34)  Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)  Urogenital Abnormalities [MESH:D014564] (2064)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Hypospadias [MESH:D007021] (798)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Angioedemas, Hereditary [MESH:D054179] (172)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Cystic Fibrosis [MESH:D003550] (760)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Diamond-Blackfan Anemia 9 [MESH:C567650] (43)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Activated Protein C Resistance [MESH:D020016] (140)  Factor XII Deficiency [MESH:D005175] (31)  Chromosome Disorders [MESH:D025063] (2030)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Down Syndrome [MESH:D004314] (1287)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Choroideremia [MESH:D015794] (18)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)  Fuchs' Endothelial Dystrophy [MESH:D005642] (86)   Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Retinitis Pigmentosa 18 [MESH:C563320] (17)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Choroideremia [MESH:D015794] (18)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Hereditary Autoinflammatory Diseases [MESH:D056660] (272)   Periodic fever, familial, autosomal dominant [MESH:C536657] (177)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62)  Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Tuberous Sclerosis [MESH:D014402] (635)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth Disease, Dominant Intermediate B [MESH:C564703] (27)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Metabolism, Inborn Errors [MESH:D008661] (6032)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis IX [MESH:C562643] (52)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Leigh Disease [MESH:D007888] (206)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Transaldolase Deficiency [MESH:C563207] (61)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 2D [MESH:C535753] (40)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Leigh Disease [MESH:D007888] (206)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Fanconi Syndrome [MESH:D005198] (253)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Muscular Dystrophies [MESH:D009136] (1597)   Bethlem myopathy [MESH:C535436] (108)  Scleroatonic muscular dystrophy [MESH:C537521] (108)  Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Epidermolysa bullosa simplex and limb girdle muscular dystrophy [MESH:C535955] (34)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2C [MESH:C535900] (20)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Tuberous Sclerosis [MESH:D014402] (635)  Peutz-Jeghers Syndrome [MESH:D010580] (51)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Skin Diseases, Genetic [MESH:D012873] (3456)   Amyloidosis IX [MESH:C562643] (52)  Stiff Skin Syndrome [MESH:C566112] (62)  Dermatitis, Atopic [MESH:D003876] (2052)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Epidermolysis Bullosa [MESH:D004820] (259)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysa bullosa simplex and limb girdle muscular dystrophy [MESH:C535955] (34)  Epidermolysis bullosa simplex, Ogna type [MESH:C535962] (34)  Epidermolysis Bullosa Simplex With Pyloric Atresia [MESH:C567408] (34)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Diabetes Mellitus, Transient Neonatal, 1 [MESH:C563322] (58)  Asphyxia Neonatorum [MESH:D001238] (1648)  Cystic Fibrosis [MESH:D003550] (760)  Ichthyosis [MESH:D007057] (476)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101) 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, Systemic [MESH:D012595] (199)  Weill-Marchesani Syndrome [MESH:D056846] (65)  Cartilage Diseases [MESH:D002357] (438)   Keutel syndrome [MESH:C536167] (102)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Marfan Syndrome [MESH:D008382] (646)   Shprintzen Golberg craniosynostosis [MESH:C537328] (76)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   MASS syndrome [MESH:C536030] (62)  Dermatomyositis [MESH:D003882] (1826)  Scleroderma, Systemic [MESH:D012595] (199)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  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)   Alopecia [MESH:D000505] (1453)   Alopecia Areata [MESH:D000506] (168)  Keratosis [MESH:D007642] (1941)   Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Lentigo [MESH:D007911] (329)   Peutz-Jeghers Syndrome [MESH:D010580] (51)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Skin Abnormalities [MESH:D012868] (1709)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysa bullosa simplex and limb girdle muscular dystrophy [MESH:C535955] (34)  Epidermolysis bullosa simplex, Ogna type [MESH:C535962] (34)  Epidermolysis Bullosa Simplex With Pyloric Atresia [MESH:C567408] (34)  Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  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)   Amyloidosis IX [MESH:C562643] (52)  Stiff Skin Syndrome [MESH:C566112] (62)  Dermatitis, Atopic [MESH:D003876] (2052)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysa bullosa simplex and limb girdle muscular dystrophy [MESH:C535955] (34)  Epidermolysis bullosa simplex, Ogna type [MESH:C535962] (34)  Epidermolysis Bullosa Simplex With Pyloric Atresia [MESH:C567408] (34)  Hereditary Autoinflammatory Diseases [MESH:D056660] (247)   Periodic fever, familial, autosomal dominant [MESH:C536657] (177)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Skin Diseases, Infectious [MESH:D012874] (2684)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)   Candidiasis familial chronic mucocutaneous, autosomal recessive [MESH:C537979] (36)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Type III [MESH:D056828] (32)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Pemphigoid, Benign Mucous Membrane [MESH:D010390] (61)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysa bullosa simplex and limb girdle muscular dystrophy [MESH:C535955] (34)  Epidermolysis bullosa simplex, Ogna type [MESH:C535962] (34)  Epidermolysis Bullosa Simplex With Pyloric Atresia [MESH:C567408] (34)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163) 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)   Mitochondrial Encephalomyopathies [MESH:D017237] (158)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Leigh Disease [MESH:D007888] (206)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)   Keutel syndrome [MESH:C536167] (102)  Aortic Valve, Calcification of [MESH:C562942] (655)  Vascular Calcification [MESH:D061205] (138)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Bloom Syndrome [MESH:D001816] (107)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Transient Neonatal, 1 [MESH:C563322] (58)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 10 [MESH:C566602] (88)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)  Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)  Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Iron Metabolism Disorders [MESH:D019189] (2139)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  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)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Malabsorption Syndromes [MESH:D008286] (1869)   Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis IX [MESH:C562643] (52)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Leigh Disease [MESH:D007888] (206)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Transaldolase Deficiency [MESH:C563207] (61)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 2D [MESH:C535753] (40)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Leigh Disease [MESH:D007888] (206)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Fanconi Syndrome [MESH:D005198] (253)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Mitochondrial Diseases [MESH:D028361] (2561)   Mitochondrial complex I deficiency [MESH:C537475] (140)  Leigh Disease [MESH:D007888] (206)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis IX [MESH:C562643] (52)  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)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypokalemia [MESH:D007008] (1041)  Hyponatremia [MESH:D007010] (789)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462) 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)   Pigmented Nodular Adrenocortical Disease, Primary, 1 [MESH:C566469] (34)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Transient Neonatal, 1 [MESH:C563322] (58)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 10 [MESH:C566602] (88)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Pituitary Neoplasms [MESH:D010911] (981)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Gonadal Disorders [MESH:D006058] (5088)   Testicular Diseases [MESH:D013733] (777)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Parathyroid Diseases [MESH:D010279] (1604)   Hypoparathyroidism [MESH:D007011] (376)   Barakat syndrome [MESH:C537907] (71)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1259)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111) 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)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)   Diabetes Mellitus, Insulin-Dependent, 10 [MESH:C566602] (88)  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)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Type III [MESH:D056828] (32)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Interleukin 2 Receptor, Alpha, Deficiency of [MESH:C565232] (88)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Positive, NK Cell-Negative [MESH:C563440] (79)  Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  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)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   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)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Salmonella Infections, Animal [MESH:D012481] (604)  Cattle Diseases [MESH:D002418] (416)   Tuberculosis, Bovine [MESH:D014380] (380)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Hernia [MESH:D006547] (2825)   Encephalocele [MESH:D004677] (151)   Knobloch syndrome [MESH:C537209] (70)  Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Hypertrophy [MESH:D006984] (4476)   Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Death [MESH:D003643] (1328)  Emphysema [MESH:D004646] (1096)  Gliosis [MESH:D005911] (1419)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Ulcer [MESH:D014456] (392)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Chromosome Aberrations [MESH:D002869] (2352)   Chromosome Breakage [MESH:D019457] (139)  Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Meier-Gorlin syndrome [MESH:C538012] (133)  Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Hemorrhage [MESH:D006470] (4451)   Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Inflammation [MESH:D007249] (5241)   Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)  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 Metastasis [MESH:D009362] (4441)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Ossification, Heterotopic [MESH:D009999] (187)   Ossification of Posterior Longitudinal Ligament [MESH:D017887] (99)   Ossification of the posterior longitudinal ligament of the spine [MESH:C537143] (98)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Sclerosis [MESH:D012598] (224)   Scleroatonic muscular dystrophy [MESH:C537521] (108)  Signs and Symptoms [MESH:D012816] (10659)   Asthenia [MESH:D001247] (376)  Chills [MESH:D023341] (644)  Edema [MESH:D004487] (3726)  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)  Neurologic Manifestations [MESH:D009461] (8702)   Gait Disorders, Neurologic [MESH:D020233] (491)  Seizures [MESH:D012640] (4502)  Dyskinesias [MESH:D020820] (3285)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Sensation Disorders [MESH:D012678] (5009)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   MYH9-Related Disorders [MESH:C535507] (46)  Macrothrombocytopenia progressive deafness [MESH:C537831] (46)  Barakat syndrome [MESH:C537907] (71)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (444)   Blindness [MESH:D001766] (178)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  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)  Hyperoxia [MESH:D018496] (694)  Respiratory Sounds [MESH:D012135] (713)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)   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)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Phencyclidine Abuse [MESH:D010623] (288)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Fractures, Bone [MESH:D050723] (597)  Heat Stress Disorders [MESH:D018882] (226)  Spinal Cord Injuries [MESH:D013119] (2688)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  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)   Organometallic Compounds [MESH:D009942] (4369)   Organotin Compounds [MESH:D009947] (166)   Trialkyltin Compounds [MESH:D014220] (42) 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) 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)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Mental Disorders [MESH:D001523] (2063)   Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Dementia [MESH:D003704] (471)   Lewy Body Disease [MESH:D020961] (139)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mental Retardation, Autosomal Dominant 3 [MESH:C567241] (14)  Mood Disorders [MESH:D019964] (257)   Affective Disorders, Psychotic [MESH:D000341] (248)   Bipolar Disorder [MESH:D001714] (247)   Major Affective Disorder 1 [MESH:C565111] (237)  Major Affective Disorder 7 [MESH:C567529] (136)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XY Disorders of Sex Development [MESH:D058490] (388)   Pseudovaginal Perineoscrotal Hypospadias [MESH:C535830] (59) G. Phenomena and Processes  G. Phenomena and Processes  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Mosaicism [MESH:D009030] (116)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  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)