Item 2 of 89 (back to results) previous next   daidzein C004742               MeSH Unique Identifier: C004742 Chemical – Gene Interaction Note 1: [Genistein co-treated with daidzein co-treated with glycitein] results in decreased expression of ABCA1 mRNA Note 2: Daidzein promotes the reaction [ABCC1 protein results in increased hydrolysis of Adenosine Triphosphate] Click here for more information

Current search: C19. Endocrine System Diseases: Endocrine System Diseases [MESH:D004700] > Adrenal Gland Diseases [MESH:D000307] > Adrenal Hyperplasia, Congenital [MESH:D000312] > Adrenal hyperplasia 2 [MESH:C538236] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Ankyrin repeat domain containing [HGNC:ANKRD] (566)   espin [HGNC:ESPN] (15)  ATPases [HGNC:ATP] (106)   ATPases, V-type [HGNC:VATP] (14)   ATPase, H+ transporting, lysosomal V0 subunit a2 [HGNC:ATP6V0A2] (10)  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily C [HGNC:ABCC] (458)   ATP-binding cassette, sub-family C (CFTR/MRP), member 1 [HGNC:ABCC1] (177)  ATP-binding cassette, sub-family C (CFTR/MRP), member 4 [HGNC:ABCC4] (88)  ATP-binding cassette, sub-family C (CFTR/MRP), member 5 [HGNC:ABCC5] (40)  Basic helix-loop-helix [HGNC:BHLH] (618)   nuclear receptor coactivator 2 [HGNC:NCOA2] (50)  v-myc avian myelocytomatosis viral oncogene homolog [HGNC:MYC] (254)  Basic leucine zipper proteins [HGNC:bZIP] (670)   FBJ murine osteosarcoma viral oncogene homolog [HGNC:FOS] (277)  jun proto-oncogene [HGNC:JUN] (290)  CD molecules [HGNC:CD] (1459)   insulin-like growth factor 1 receptor [HGNC:IGF1R] (72)  lysosomal-associated membrane protein 3 [HGNC:LAMP3] (37)  solute carrier family 07 (amino acid transporter light chain, L system), member 05 [HGNC:SLC7A5] (51)  vascular cell adhesion molecule 1 [HGNC:VCAM1] (172)  Cyclin-dependent kinases [HGNC:CDK] (338)   cyclin-dependent kinase 02 [HGNC:CDK2] (177)  cyclin-dependent kinase 04 [HGNC:CDK4] (127)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566)  cytochrome P450, family 01, subfamily B, polypeptide 01 [HGNC:CYP1B1] (301)  cytochrome P450, family 02, subfamily C, polypeptide 09 [HGNC:CYP2C9] (220)  cytochrome P450, family 02, subfamily D, polypeptide 06 [HGNC:CYP2D6] (200)  cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612)  cytochrome P450, family 19, subfamily A, polypeptide 01 [HGNC:CYP19A1] (210)  cytochrome P450, family 21, subfamily A, polypeptide 02 [HGNC:CYP21A2] (40)  Endogenous Ligands [HGNC:ENDOLIG] (1191)   chemokine (C-X-C motif) ligand 12 [HGNC:CXCL12] (70)  interleukin 08 [HGNC:IL8] (649)  EPH receptors [HGNC:EPH] (55)   EPH receptor A1 [HGNC:EPHA1] (21)  Fibronectin type III domain containing [HGNC:FN3] (399)   EPH receptor A1 [HGNC:EPHA1] (21)  insulin-like growth factor 1 receptor [HGNC:IGF1R] (72)  Homeoboxes [HGNC:homeobox] (219)   Homeoboxes, ANTP class [HGNC:HOXL] (152)   NKL subclass homeoboxes [HGNC:NKL] (109)   NK3 homeobox 1 [HGNC:NKX3-1] (42)  Immunoglobulin superfamily domain containing [HGNC:IGSF] (761)   C2-set domain containing [HGNC:C2SET] (225)   vascular cell adhesion molecule 1 [HGNC:VCAM1] (172)  I-set domain containing [HGNC:ISET] (447)   vascular cell adhesion molecule 1 [HGNC:VCAM1] (172)  Immunoglobulin-like domain containing [HGNC:IGD] (645)   vascular cell adhesion molecule 1 [HGNC:VCAM1] (172)  Interferons and interferon receptors [HGNC:IFN] (684)   interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 01, beta [HGNC:IL1B] (497)  interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)  interleukin 08 [HGNC:IL8] (649)  K-acetyltransferases [HGNC:KAT] (176)   nuclear receptor coactivator 2 [HGNC:NCOA2] (50)  Metallothioneins [HGNC:MT] (183)   metallothionein 2A [HGNC:MT2A] (133)  Mitogen-activated protein kinase cascade [HGNC:MAP#K] (854)   Mitogen-activated protein kinases [HGNC:MAPK] (797)   mitogen-activated protein kinase 01 [HGNC:MAPK1] (651)  mitogen-activated protein kinase 03 [HGNC:MAPK3] (644)  Nuclear hormone receptors [HGNC:NR] (1322)   estrogen receptor 1 [HGNC:ESR1] (506)  estrogen receptor 2 (ER beta) [HGNC:ESR2] (261)  estrogen-related receptor alpha [HGNC:ESRRA] (30)  estrogen-related receptor beta [HGNC:ESRRB] (8)  nuclear receptor subfamily 1, group I, member 2 [HGNC:NR1I2] (328)  progesterone receptor [HGNC:PGR] (209)  Parkinson disease [HGNC:PARK] (136)   ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase) [HGNC:UCHL1] (27)  Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225)   Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155)   protein tyrosine kinase 2 [HGNC:PTK2] (77)  Short chain dehydrogenase/reductase superfamily [HGNC:SDR] (302)   Short chain dehydrogenase/reductase superfamily, Extended fold [HGNC:SDRE] (92)   hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 [HGNC:HSD3B2] (55)  Solute carriers [HGNC:SLC] (716)   solute carrier family 02 (facilitated glucose transporter), member 01 [HGNC:SLC2A1] (80)  solute carrier family 07 (amino acid transporter light chain, L system), member 05 [HGNC:SLC7A5] (51)  solute carrier family 12 (sodium/potassium/chloride transporter), member 2 [HGNC:SLC12A2] (26)  Sterile alpha motif (SAM) containing [HGNC:SAMD] (92)   EPH receptor A1 [HGNC:EPHA1] (21)  Sulfotransferases, cytosolic [HGNC:SULT] (167)   sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 [HGNC:SULT1A1] (105)  Tachykinin receptors [HGNC:TACR] (24)   tachykinin receptor 3 [HGNC:TACR3] (6)  UDP glucuronosyltransferases [HGNC:UGT] (298)   UDP glucuronosyltransferase 1 family, polypeptide A1 [HGNC:UGT1A1] (167)  UDP glucuronosyltransferase 1 family, polypeptide A9 [HGNC:UGT1A9] (108)  UDP glucuronosyltransferase 2 family, polypeptide B17 [HGNC:UGT2B17] (20) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   activity (338)  binding (2423)  chemical synthesis (83)  cotreatment (1499)  expression (494)  reaction (624)  response to substance (623)  transport (172)  Decreases (5154)   activity (2549)  expression (2187)  reaction (3393)  response to substance (713)  Increases (5571)   activity (2865)  cleavage (666)  export (105)  expression (3238)  glucuronidation (189)  hydrolysis (158)  methylation (105)  phosphorylation (1060)  reaction (1574)  secretion (901)  sulfation (74) A. Anatomy  A. Anatomy  Sense Organs [MESH:D012679] (1060)   Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Peters anomaly [MESH:C537884] (465)  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, 16-18 [MESH:D002902] (799)   Chromosomes, Human, Pair 17 [MESH:D002886] (779)   Chromosome 17 deletion [MESH:C538045] (769) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Pasteurellaceae Infections [MESH:D016871] (348)  Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)  Paratuberculosis [MESH:D010283] (427)  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)  Urinary Tract Infections [MESH:D014552] (984)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Skin Diseases, Infectious [MESH:D012874] (415)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289)  Mycoses [MESH:D009181] (385)   Candidiasis [MESH:D002177] (307)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Herpesviridae Infections [MESH:D006566] (1944)   Cytomegalovirus Infections [MESH:D003586] (222)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  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)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   HIV Wasting Syndrome [MESH:D019247] (1956)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   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)   Malaria [MESH:D008288] (2175)  Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Hamartoma [MESH:D006222] (1484)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Myeloid [MESH:D007951] (2773)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Hepatoblastoma [MESH:D018197] (548)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Liposarcoma [MESH:D008080] (612)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Aggressive [MESH:D018222] (1562)  Histiocytoma [MESH:D051642] (272)   Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Leiomyosarcoma [MESH:D007890] (977)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Embryonal [MESH:D018233] (98)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Leiomyosarcoma [MESH:D007890] (977)  Liposarcoma [MESH:D008080] (612)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Embryonal [MESH:D018233] (98)  Phyllodes Tumor [MESH:D003557] (113)   Phyllodes Tumor of the Prostate [MESH:C549759] (110)  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)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Mesothelioma [MESH:D008654] (2567)  Prolactinoma [MESH:D015175] (312)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Gonadal Tissue [MESH:D018309] (284)   Sex Cord-Gonadal Stromal Tumors [MESH:D018312] (282)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  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)   Bone Neoplasms [MESH:D001859] (1334)  Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   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)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Thyroid Neoplasms [MESH:D013964] (2040)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Thyroid Neoplasms [MESH:D013964] (2040)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  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)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Invasiveness [MESH:D009361] (3388)   Leukemic Infiltration [MESH:D017254] (5)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Precancerous Conditions [MESH:D011230] (2858)   Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Bone Diseases, Developmental [MESH:D001848] (3315)   Dwarfism [MESH:D004392] (778)   Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Osteochondrodysplasias [MESH:D010009] (2440)   Fibrous Dysplasia of Bone [MESH:D005357] (737)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Resorption [MESH:D001862] (2352)   Alveolar Bone Loss [MESH:D016301] (220)  Osteolysis [MESH:D010014] (1787)  Spinal Diseases [MESH:D013122] (2485)   Spinal Curvatures [MESH:D013121] (742)   Kyphosis [MESH:D007738] (637)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Joint Diseases [MESH:D007592] (4657)   Ankylosis [MESH:D000844] (479)   Spondylitis, Ankylosing [MESH:D013167] (431)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Muscular Diseases [MESH:D009135] (4071)   Muscle Rigidity [MESH:D009127] (617)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Microcephaly [MESH:D008831] (700)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Bile Duct Neoplasms [MESH:D001650] (367)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Deglutition Disorders [MESH:D003680] (1538)   Esophageal Motility Disorders [MESH:D015154] (1489)   Gastroesophageal Reflux [MESH:D005764] (1465)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Esophagitis [MESH:D004941] (1120)   Esophagitis, Peptic [MESH:D004942] (709)  Gastroenteritis [MESH:D005759] (4066)   Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Esophagitis [MESH:D004941] (1120)   Esophagitis, Peptic [MESH:D004942] (709)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Intestinal Perforation [MESH:D007416] (471)  Cecal Diseases [MESH:D002429] (1330)   Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   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)  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)   Duodenal Ulcer [MESH:D004381] (1549)  Esophagitis, Peptic [MESH:D004942] (709)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatomegaly [MESH:D006529] (1169)  Hypertension, Portal [MESH:D006975] (869)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis, Viral, Human [MESH:D006525] (1766)   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)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   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)   Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572) 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)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Periodontal Diseases [MESH:D010510] (1001)   Periodontal Atrophy [MESH:D055093] (225)   Alveolar Bone Loss [MESH:D016301] (220)  Periodontitis [MESH:D010518] (843)   Chronic Periodontitis [MESH:D055113] (231)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  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)   Bronchiectasis [MESH:D001987] (1792)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Lung Diseases [MESH:D008171] (7249)   Hypertension, Pulmonary [MESH:D006976] (2000)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Hyperventilation [MESH:D006985] (654)  Respiratory Insufficiency [MESH:D012131] (841)  Apnea [MESH:D001049] (748)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Rhinitis [MESH:D012220] (766)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Deafness, Autosomal Recessive 35 [MESH:C563908] (17)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Chronobiology Disorders [MESH:D021081] (970)  Sleep Disorders [MESH:D012893] (2050)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Myasthenia Gravis [MESH:D009157] (632)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Central Nervous System Diseases [MESH:D002493] (9745)   Meningitis [MESH:D008581] (352)  Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Kernicterus [MESH:D007647] (256)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 14 [MESH:C537196] (49)  Spinocerebellar Ataxias [MESH:D020754] (322)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  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)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Hypopituitarism [MESH:D007018] (732)  Hyperpituitarism [MESH:D006964] (1250)   Hyperprolactinemia [MESH:D006966] (603)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis [MESH:D008581] (1506)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Movement Disorders [MESH:D009069] (4823)   Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 14 [MESH:C537196] (49)  Spinocerebellar Ataxias [MESH:D020754] (322)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Multiple Sclerosis [MESH:D009103] (1716)  Nervous System Malformations [MESH:D009421] (3354)   Neural Tube Defects [MESH:D009436] (2143)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurocutaneous Syndromes [MESH:D020752] (1230)   von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  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 ataxia 14 [MESH:C537196] (49)  Spinocerebellar Ataxias [MESH:D020754] (322)  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)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Tremor [MESH:D014202] (840)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Consciousness Disorders [MESH:D003244] (680)   Unconsciousness [MESH:D014474] (660)   Coma [MESH:D003128] (524)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Coffin-Lowry Syndrome [MESH:D038921] (45)  Neuromuscular Manifestations [MESH:D020879] (2130)   Spasm [MESH:D013035] (418)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Pain, Intractable [MESH:D010148] (707)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Reflex, Abnormal [MESH:D012021] (485)   Reflex, Babinski [MESH:D001405] (97)  Sensation Disorders [MESH:D012678] (5011)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Deafness, Autosomal Recessive 35 [MESH:C563908] (17)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Muscular Diseases [MESH:D009135] (3538)   Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)   Neuralgia, Postherpetic [MESH:D051474] (742)  Polyneuropathies [MESH:D011115] (1134)   Tangier Disease [MESH:D013631] (170)  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)   Corneal Diseases [MESH:D003316] (1445)   Corneal Opacity [MESH:D003318] (544)   Peters anomaly [MESH:C537884] (465)  Eye Abnormalities [MESH:D005124] (1233)   Peters anomaly [MESH:C537884] (465)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Albinism [MESH:D000417] (258)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma 3, Primary Congenital, A [MESH:C565547] (434)  Glaucoma, Open-Angle [MESH:D005902] (1281)   Glaucoma, Primary Open Angle [MESH:C562750] (466)  Glaucoma 1, Open Angle, A [MESH:C564234] (446)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 9 [MESH:C566958] (149)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Aromatase deficiency [MESH:C537436] (277)  Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)  Penile Diseases [MESH:D010409] (1805)   Penile Neoplasms [MESH:D010412] (890)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Hyperplasia [MESH:D011470] (336)  Prostatic Neoplasms [MESH:D011471] (6135)   Phyllodes Tumor of the Prostate [MESH:C549759] (110)  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)   Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MESH:C535979] (43)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Sexual Dysfunction, Physiological [MESH:D012735] (270)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   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 Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Abnormalities [MESH:D014564] (2043)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MESH:C535979] (43)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Fetal Diseases [MESH:D005315] (1206)   Chorioamnionitis [MESH:D002821] (313)  Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Abruptio Placentae [MESH:D000037] (430)  Obstetric Labor, Premature [MESH:D007752] (1316)  Fetal Membranes, Premature Rupture [MESH:D005322] (356)   Chorioamnionitis [MESH:D002821] (313)  Placenta Diseases [MESH:D010922] (1781)   Abruptio Placentae [MESH:D000037] (430)  Chorioamnionitis [MESH:D002821] (313)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870)  Puerperal Disorders [MESH:D011644] (324)   Lactation Disorders [MESH:D007775] (235)   Galactorrhea [MESH:D005687] (233) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Vascular Malformations [MESH:D054079] (1098)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Heart Diseases [MESH:D006331] (8614)   Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Pericardial Effusion [MESH:D010490] (1015)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Cardiac Complexes, Premature [MESH:D005117] (429)   Ventricular Premature Complexes [MESH:D018879] (418)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Heart Defects, Congenital [MESH:D006330] (2443)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Vasospasm [MESH:D003329] (533)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Arteritis [MESH:D001167] (1084)  Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Peripheral Vascular Diseases [MESH:D016491] (1412)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Thrombosis [MESH:D013927] (3101)  Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Pregnancy-Induced [MESH:D046110] (397)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Vasospasm [MESH:D003329] (533)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084)  Behcet Syndrome [MESH:D001528] (1784)  Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Purpura, Schoenlein-Henoch [MESH:D011695] (266) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Methemoglobinemia [MESH:D008708] (850)  Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Hemolytic [MESH:D000743] (3083)   Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Kernicterus [MESH:D007647] (256)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Blood Protein Disorders [MESH:D001796] (3051)   Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Leukocyte Disorders [MESH:D007960] (2662)   Leukocytosis [MESH:D007964] (988)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Thrombophilia [MESH:D019851] (592)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Lymphatic Diseases [MESH:D008206] (5167)   Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Splenic Diseases [MESH:D013158] (1323)  Lymphatic Abnormalities [MESH:D044148] (251)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Drug-Induced [MESH:D000014] (1024)  Abnormalities, Multiple [MESH:D000015] (3192)   Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)  Down Syndrome [MESH:D004314] (1287)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Ectodermal Dysplasia [MESH:D004476] (938)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Vascular Malformations [MESH:D054079] (1108)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1018)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Chromosome Disorders [MESH:D025063] (2030)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Down Syndrome [MESH:D004314] (1287)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Eye Abnormalities [MESH:D005124] (1233)   Peters anomaly [MESH:C537884] (465)  Lymphatic Abnormalities [MESH:D044148] (251)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Microcephaly [MESH:D008831] (700)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Nervous System Malformations [MESH:D009421] (3354)   Neural Tube Defects [MESH:D009436] (2143)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Skin Abnormalities [MESH:D012868] (1723)   Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  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)   Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MESH:C535979] (43)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Fetal Diseases [MESH:D005315] (1205)   Chorioamnionitis [MESH:D002821] (313)  Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MESH:C535979] (43)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Chromosome Disorders [MESH:D025063] (2030)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Down Syndrome [MESH:D004314] (1287)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Dwarfism [MESH:D004392] (783)   Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Coffin-Lowry Syndrome [MESH:D038921] (45)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Coffin-Lowry Syndrome [MESH:D038921] (45)  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 ataxia 14 [MESH:C537196] (49)  Spinocerebellar Ataxias [MESH:D020754] (322)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Aromatase deficiency [MESH:C537436] (277)  Coumarin Resistance [MESH:C563039] (397)  Drug Metabolism, Poor, CYP2D6-Related [MESH:C563835] (220)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Hyperhomocysteinemia [MESH:D020138] (1724)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease XIII [MESH:C567861] (52)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Gilbert Disease [MESH:D005878] (259)  Crigler-Najjar Syndrome [MESH:D003414] (255)   Crigler Najjar syndrome, type 2 [MESH:C536213] (254)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (365)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hypophosphatasia [MESH:D007014] (142)   Hypophosphatasia, Childhood [MESH:C562440] (137)  Hypophosphatasia, Infantile [MESH:C562646] (137)  Hypophosphatasia, Adult [MESH:C562647] (137)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MESH:C535979] (43)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Cutis Laxa [MESH:D003483] (177)   Wrinkly skin syndrome [MESH:C536750] (24)  Cutis Laxa, Autosomal Recessive, Type IIA [MESH:C562632] (24)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Erythroblastosis, Fetal [MESH:D004899] (257)   Kernicterus [MESH:D007647] (256)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Scleroderma, Localized [MESH:D012594] (1597)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Cutis Laxa [MESH:D003483] (177)   Wrinkly skin syndrome [MESH:C536750] (24)  Cutis Laxa, Autosomal Recessive, Type IIA [MESH:C562632] (24)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Keratosis [MESH:D007642] (1941)  Scleroderma, Localized [MESH:D012594] (1597)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Gynecomastia [MESH:D006177] (484)   Aromatase deficiency [MESH:C537436] (277)  Lactation Disorders [MESH:D007775] (235)   Galactorrhea [MESH:D005687] (233)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  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)  Photosensitivity Disorders [MESH:D010787] (272)   Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)  Pigmentation Disorders [MESH:D010859] (1215)   Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)  Skin Abnormalities [MESH:D012868] (1709)   Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Dermatitis, Atopic [MESH:D003876] (2052)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Cutis Laxa [MESH:D003483] (177)   Wrinkly skin syndrome [MESH:C536750] (24)  Cutis Laxa, Autosomal Recessive, Type IIA [MESH:C562632] (24)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)  Skin Diseases, Infectious [MESH:D012874] (2684)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Urticaria [MESH:D014581] (2668)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Pemphigoid, Bullous [MESH:D010391] (707)  Pemphigus [MESH:D010392] (158)  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)   Hepatic Encephalopathy [MESH:D006501] (1795)  Kernicterus [MESH:D007647] (256)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Hypercalcemia [MESH:D006934] (1999)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Fanconi Anemia [MESH:D005199] (1604)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Cockayne Syndrome [MESH:D003057] (107)   Cerebrooculofacioskeletal Syndrome 1 [MESH:C562434] (72)  Xeroderma Pigmentosum [MESH:D014983] (213)   Xeroderma Pigmentosum, Complementation Group G [MESH:C562593] (54)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hypertriglyceridemia [MESH:D015228] (808)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (409)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Malabsorption Syndromes [MESH:D008286] (1869)   Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Aromatase deficiency [MESH:C537436] (277)  Coumarin Resistance [MESH:C563039] (397)  Drug Metabolism, Poor, CYP2D6-Related [MESH:C563835] (220)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Hyperhomocysteinemia [MESH:D020138] (1724)  Albinism [MESH:D000417] (359)   Albinism, Ocular [MESH:D016117] (157)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Albinism, Oculocutaneous [MESH:D016115] (234)   Oculocutaneous albinism type 1 [MESH:C537728] (110)  Oculocutaneous albinism type 1B [MESH:C537729] (110)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease XIII [MESH:C567861] (52)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Gilbert Disease [MESH:D005878] (259)  Crigler-Najjar Syndrome [MESH:D003414] (255)   Crigler Najjar syndrome, type 2 [MESH:C536213] (254)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (365)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hypophosphatasia [MESH:D007014] (142)   Hypophosphatasia, Childhood [MESH:C562440] (137)  Hypophosphatasia, Infantile [MESH:C562646] (137)  Hypophosphatasia, Adult [MESH:C562647] (137)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MESH:C535979] (43)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Mitochondrial Diseases [MESH:D028361] (2561)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Proteostasis Deficiencies [MESH:D057165] (3522)   TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hyponatremia [MESH:D007010] (789)  Water Intoxication [MESH:D014869] (106)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)  Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MESH:C535979] (43)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Thyroid Neoplasms [MESH:D013964] (2040)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Delayed [MESH:D011628] (449)  Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Congenital adrenal hyperplasia due to 21 hydroxylase deficiency [MESH:C535979] (43)  Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypogonadism [MESH:D007006] (1123)   Sexual Infantilism [MESH:D050035] (277)  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)  Testicular Diseases [MESH:D013733] (777)   Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Hypoparathyroidism [MESH:D007011] (376)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Pituitary Diseases [MESH:D010900] (1829)   Hypopituitarism [MESH:D007018] (732)  Hyperpituitarism [MESH:D006964] (1259)   Hyperprolactinemia [MESH:D006966] (603)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Pemphigoid, Bullous [MESH:D010391] (707)  Pemphigus [MESH:D010392] (158)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Myasthenia Gravis [MESH:D009157] (632)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Kernicterus [MESH:D007647] (256)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  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)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Dermatitis, Atopic [MESH:D003876] (2052)  Urticaria [MESH:D014581] (2668)  Food Hypersensitivity [MESH:D005512] (608)   Peanut Hypersensitivity [MESH:D021183] (572)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immune Complex Diseases [MESH:D007105] (782)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Lymphopenia [MESH:D008231] (990)  HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  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)  Paratuberculosis [MESH:D010283] (427)  Cattle Diseases [MESH:D002418] (416)   Tuberculosis, Bovine [MESH:D014380] (380) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Atrophy [MESH:D001284] (2603)  Plaque, Atherosclerotic [MESH:D058226] (696)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Hypertrophy [MESH:D006984] (4476)   Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Emphysema [MESH:D004646] (1096)  Gliosis [MESH:D005911] (1419)  Hyperplasia [MESH:D006965] (2463)  Leukocytosis [MESH:D007964] (978)  Lithiasis [MESH:D020347] (345)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Cardiac Complexes, Premature [MESH:D005117] (429)   Ventricular Premature Complexes [MESH:D018879] (418)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  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)   Chromosome 17 deletion [MESH:C538045] (769)  Death [MESH:D003643] (1328)   Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Disease Attributes [MESH:D020969] (3654)   Critical Illness [MESH:D016638] (296)  Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Hyperbilirubinemia [MESH:D006932] (1860)   Kernicterus [MESH:D007647] (256)  Hyperbilirubinemia, Neonatal [MESH:D051556] (258)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Ischemia [MESH:D007511] (3049)   Infarction [MESH:D007238] (298)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Dysmenorrhea [MESH:D004412] (189)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)  Necrosis [MESH:D009336] (4019)   Infarction [MESH:D007238] (298)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Invasiveness [MESH:D009361] (3388)   Leukemic Infiltration [MESH:D017254] (5)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Edema [MESH:D004487] (3726)  Feminization [MESH:D005262] (655)  Fetal Distress [MESH:D005316] (99)  Flushing [MESH:D005483] (506)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Ataxia [MESH:D001259] (984)  Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Tremor [MESH:D014202] (840)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Consciousness Disorders [MESH:D003244] (677)   Unconsciousness [MESH:D014474] (657)   Coma [MESH:D003128] (492)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Neuromuscular Manifestations [MESH:D020879] (2130)   Spasm [MESH:D013035] (418)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Pain, Intractable [MESH:D010148] (707)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2298)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Reflex, Abnormal [MESH:D012021] (485)   Reflex, Babinski [MESH:D001405] (97)  Sensation Disorders [MESH:D012678] (5009)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Albinism ocular late onset sensorineural deafness [MESH:C537043] (137)  Deafness, Autosomal Recessive 35 [MESH:C563908] (17)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Pain, Intractable [MESH:D010148] (707)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Pelvic Pain [MESH:D017699] (198)   Dysmenorrhea [MESH:D004412] (189)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Diarrhea [MESH:D003967] (858)  Nausea [MESH:D009325] (2300)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperoxia [MESH:D018496] (694)  Hyperventilation [MESH:D006985] (652)  Respiratory Sounds [MESH:D012135] (713)  Apnea [MESH:D001049] (415)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Skin Manifestations [MESH:D012877] (1250)   Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Urological Manifestations [MESH:D020924] (3532)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  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)  Water Intoxication [MESH:D014869] (106)  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)  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)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Morphine Dependence [MESH:D009021] (855) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  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)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D03. Heterocyclic Compounds  D03. Heterocyclic Compounds  Heterocyclic Compounds [MESH:D006571] (56330)   Heterocyclic Compounds, 2-Ring [MESH:D006574] (24204)   Benzopyrans [MESH:D001578] (5622)   Chromones [MESH:D002867] (3329)   Flavonoids [MESH:D005419] (3001)   Isoflavones [MESH:D007529] (486)  Pyrans [MESH:D011714] (6850)   Benzopyrans [MESH:D001578] (5610)   Chromones [MESH:D002867] (3317)   Flavonoids [MESH:D005419] (2989)   Isoflavones [MESH:D007529] (483) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Mental Disorders [MESH:D001523] (2063)   Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XX Disorders of Sex Development [MESH:D058489] (375)   Aromatase deficiency [MESH:C537436] (277) 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)   Chromosome 17 deletion [MESH:C538045] (769)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 16-18 [MESH:D002902] (799)   Chromosomes, Human, Pair 17 [MESH:D002886] (779)   Chromosome 17 deletion [MESH:C538045] (769)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Mosaicism [MESH:D009030] (116)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)