Item 20 of 111 (back to results) previous next   cupric oxide C030973               MeSH Unique Identifier: C030973 Chemical – Gene Interaction Note 1: Cupric oxide results in decreased expression of ABCB10 mRNA Note 2: Cupric oxide results in increased expression of ACRC mRNA Click here for more information

Current search: C20. Immune System Diseases: Immune System Diseases [MESH:D007154] > Hypersensitivity [MESH:D006967] > Hypersensitivity, Immediate [MESH:D006969] > Urticaria [MESH:D014581] > Angioedema [MESH:D000799] > Angioedemas, Hereditary [MESH:D054179] > Hereditary Angioedema Types I and II [MESH:D056829] × 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)   death-associated protein kinase 1 [HGNC:DAPK1] (42)  euchromatic histone-lysine N-methyltransferase 1 [HGNC:EHMT1] (11)  Basic helix-loop-helix [HGNC:BHLH] (618)   hairy and enhancer of split 1 (Drosophila) [HGNC:HES1] (41)  hairy/enhancer-of-split related with YRPW motif 1 [HGNC:HEY1] (25)  MAX interactor 1, dimerization protein [HGNC:MXI1] (19)  single-minded homolog 2 (Drosophila) [HGNC:SIM2] (2)  sterol regulatory element binding transcription factor 2 [HGNC:SREBF2] (32)  v-myc avian myelocytomatosis viral oncogene homolog [HGNC:MYC] (254)  Basic leucine zipper proteins [HGNC:bZIP] (670)   cAMP responsive element modulator [HGNC:CREM] (36)  FBJ murine osteosarcoma viral oncogene homolog [HGNC:FOS] (277)  FBJ murine osteosarcoma viral oncogene homolog B [HGNC:FOSB] (45)  CD molecules [HGNC:CD] (1459)   v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2 [HGNC:ERBB2] (109)  Collagens [HGNC:COL] (230)   collagen, type IV, alpha 1 [HGNC:COL4A1] (18)  collagen, type V, alpha 1 [HGNC:COL5A1] (17)  collagen, type V, alpha 2 [HGNC:COL5A2] (22)  Cyclin-dependent kinases [HGNC:CDK] (338)   cyclin-dependent kinase 01 [HGNC:CDK1] (151)  cyclin-dependent kinase 06 [HGNC:CDK6] (55)  EPH receptors [HGNC:EPH] (55)   EPH receptor B2 [HGNC:EPHB2] (12)  Fibrinogen C domain containing [HGNC:FIBC] (113)   angiopoietin-like 4 [HGNC:ANGPTL4] (40)  Fibronectin type III domain containing [HGNC:FN3] (399)   EPH receptor B2 [HGNC:EPHB2] (12)  Fibulins [HGNC:FBLN] (53)   EGF containing fibulin-like extracellular matrix protein 1 [HGNC:EFEMP1] (24)  F-boxes [HGNC:FBX] (66)   F-boxes and leucine-rich repeats [HGNC:FBXL] (58)   F-box and leucine-rich repeat protein 19 [HGNC:FBXL19] (1)  Heat shock proteins [HGNC:HSP] (390)   Heat shock proteins, HSP70 [HGNC:HSP70] (294)   heat shock 105kDa/110kDa protein 01 [HGNC:HSPH1] (45)  Heat shock proteins, DNAJ (HSP40) [HGNC:DNAJ] (88)   DnaJ (Hsp40) homolog, subfamily A, member 01 [HGNC:DNAJA1] (38)  DnaJ (Hsp40) homolog, subfamily B, member 06 [HGNC:DNAJB6] (23)  DnaJ (Hsp40) homolog, subfamily C, member 03 [HGNC:DNAJC3] (22)  Heat shock proteins, HSPB (small) [HGNC:HSPB] (127)   crystallin, alpha B [HGNC:CRYAB] (42)  heat shock 22kDa protein 08 [HGNC:HSPB8] (28)  Heat shock proteins, HSPC (HSP90) [HGNC:HSP90] (119)   heat shock protein 90kDa alpha (cytosolic), class A member 1 [HGNC:HSP90AA1] (60)  High mobility group [HGNC:HMG] (101)   High mobility group, Canonical [HGNC:HMG] (98)   high mobility group box 2 [HGNC:HMGB2] (37)  Histamine receptors [HGNC:HRH] (86)   histamine receptor H1 [HGNC:HRH1] (44)  Histones [HGNC:HIST] (173)   Histones, Replication-independent [HGNC:RIH] (148)   H2A histone family, member X [HGNC:H2AFX] (129)  Homeoboxes [HGNC:homeobox] (219)   Homeoboxes, PRD class [HGNC:PRD] (60)   PROP paired-like homeobox 1 [HGNC:PROP1] (3)  Immunoglobulin superfamily domain containing [HGNC:IGSF] (761)   I-set domain containing [HGNC:ISET] (447)   obscurin-like 1 [HGNC:OBSL1] (12)  Immunoglobulin-like domain containing [HGNC:IGD] (645)   obscurin-like 1 [HGNC:OBSL1] (12)  Intermediate filaments [HGNC:IF] (273)   Type V. Lamins [HGNC:] (81)   lamin B1 [HGNC:LMNB1] (50)  lamin B2 [HGNC:LMNB2] (17)  K-methyltransferases [HGNC:KMT] (101)   euchromatic histone-lysine N-methyltransferase 1 [HGNC:EHMT1] (11)  MAX dimerization proteins [HGNC:MXD] (65)   MAX interactor 1, dimerization protein [HGNC:MXI1] (19)  Metallothioneins [HGNC:MT] (183)   metallothionein 1A [HGNC:MT1A] (54)  metallothionein 1G [HGNC:MT1G] (56)  metallothionein 2A [HGNC:MT2A] (133)  Myosins [HGNC:myosin] (111)   Myosins, class I [HGNC:MYOI] (30)   myosin IB [HGNC:MYO1B] (20)  Myosins, class II [HGNC:MYHII] (61)   myosin, heavy chain 09, non-muscle [HGNC:MYH9] (16)  Myosins, class V [HGNC:MYOV] (27)   myosin VC [HGNC:MYO5C] (9)  Nuclear hormone receptors [HGNC:NR] (1322)   nuclear receptor subfamily 2, group F, member 2 [HGNC:NR2F2] (22)  nuclear receptor subfamily 4, group A, member 1 [HGNC:NR4A1] (68)  nuclear receptor subfamily 4, group A, member 3 [HGNC:NR4A3] (35)  Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227)   insulin receptor substrate 1 [HGNC:IRS1] (47)  spectrin, beta, non-erythrocytic 1 [HGNC:SPTBN1] (28)  TRIO and F-actin binding protein [HGNC:TRIOBP] (16)  Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225)   Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155)   aurora kinase A [HGNC:AURKA] (52)  aurora kinase B [HGNC:AURKB] (47)  Protein tyrosine phosphatases, including dual specificity phosphatases [HGNC:PTP] (254)   Protein tyrosine phosphatases, Class I Cys-based [HGNC:PTPN] (252)   Class I Cys-based PTPs : Non-receptor [HGNC:PTPN] (75)   protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase) [HGNC:PTPN13] (22)  Protocadherins [HGNC:PCDH] (22)   Protocadherins, non-clustered [HGNC:PCDHN] (22)   protocadherin 09 [HGNC:PCDH9] (12)  Rho GTPase activating proteins [HGNC:ARHGAP] (76)   deleted in liver cancer 1 [HGNC:DLC1] (22)  Rho guanine nucleotide exchange factors [HGNC:ARHGEF] (105)   amyotrophic lateral sclerosis 2 (juvenile) [HGNC:ALS2] (13)  Secreted frizzled-related proteins [HGNC:SFRP] (46)   secreted frizzled-related protein 1 [HGNC:SFRP1] (21)  SH2 domain containing [HGNC:SH2D] (431)   breast cancer anti-estrogen resistance 3 [HGNC:BCAR3] (25)  Snail homologs [HGNC:SNAI] (56)   snail family zinc finger 1 [HGNC:SNAI1] (41)  Specificity protein transcription factors [HGNC:SP] (109)   Sp1 transcription factor [HGNC:SP1] (106)  SRY (sex determining region Y)-boxes [HGNC:SOX] (95)   SRY (sex determining region Y)-box 08 [HGNC:SOX8] (7)  StAR-related lipid transfer (START) domain containing [HGNC:STARD] (91)   deleted in liver cancer 1 [HGNC:DLC1] (22)  Sterile alpha motif (SAM) containing [HGNC:SAMD] (92)   EPH receptor B2 [HGNC:EPHB2] (12)  Tetratricopeptide repeat domain containing [HGNC:TTC] (153)   DnaJ (Hsp40) homolog, subfamily C, member 03 [HGNC:DNAJC3] (22)  G-protein signaling modulator 2 [HGNC:GPSM2] (27)  Tropomyosins [HGNC:TPM] (66)   tropomyosin 1 (alpha) [HGNC:TPM1] (32)  ZINC FINGERS [HGNC:ZNF] (383)   Zinc fingers, C2H2-type [HGNC:ZNF] (349)   early growth response 1 [HGNC:EGR1] (140)  pleiomorphic adenoma gene-like 1 [HGNC:PLAGL1] (20)  snail family zinc finger 1 [HGNC:SNAI1] (41)  Sp1 transcription factor [HGNC:SP1] (106)  Zinc fingers, C2H2-type with KRAB domain [HGNC:ZKRAB] (42)   zinc finger protein 331 [HGNC:ZNF331] (8)  Other zinc fingers [HGNC:] (148)   Zinc fingers, C2CH-type [HGNC:THAP domain containing] (5)   THAP domain containing, apoptosis associated protein 1 [HGNC:THAP1] (5) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   cotreatment (1499)  Decreases (5154)   activity (2549)  expression (2187)  response to substance (713)  Increases (5571)   expression (3238)  reaction (1574) 4. Semantic Terms  4. Semantic Terms  Entity [STY:T071] (48056)   Physical Object [STY:T072] (47583)   Substance [STY:T167] (46174)   Chemical [STY:T103] (46110)   Chemical Viewed Functionally [STY:T120] (28747)   Pharmacologic Substance [STY:T121] (11019)  Chemical Viewed Structurally [STY:T104] (44741)   Inorganic Chemical [STY:T197] (530) A. Anatomy  A. Anatomy  Cardiovascular System [MESH:D002319] (1086)   Blood Vessels [MESH:D001808] (278)   Arteries [MESH:D001158] (173)   Retinal Artery [MESH:D012161] (78)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Retinal Vessels [MESH:D012171] (112)   Retinal Artery [MESH:D012161] (78)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Nervous System [MESH:D009420] (587)   Central Nervous System [MESH:D002490] (371)   Hydrolethalus Syndrome 1 [MESH:C565504] (14)  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, 6-12 and X [MESH:D002906] (120)   Chromosomes, Human, Pair 9 [MESH:D002899] (40)   Kleefstra Syndrome [MESH:C563043] (25)  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)   Helicobacter Infections [MESH:D016481] (579)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)   Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  RNA Virus Infections [MESH:D012327] (4215)   Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)  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) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myeloid, Acute [MESH:D015470] (2176)  Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative [MESH:D054438] (18)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Lymphatic Vessel Tumors [MESH:D018190] (171)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Hepatoblastoma [MESH:D018197] (548)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  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)   Adenoma, Liver Cell [MESH:D018248] (685)  Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   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, 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, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  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)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Breast Neoplasms [MESH:D001943] (6077)  Skin Neoplasms [MESH:D012878] (2992)  Digestive System Neoplasms [MESH:D004067] (7487)   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)   Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   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)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  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)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Wilms Tumor [MESH:D009396] (553)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Diseases, Developmental [MESH:D001848] (3315)   Dwarfism [MESH:D004392] (778)   Seckel syndrome 1 [MESH:C537533] (63)  Three M Syndrome 2 [MESH:C567862] (22)  Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 2 [MESH:C563172] (35)  Osteochondrodysplasias [MESH:D010009] (2440)   Fibrous Dysplasia of Bone [MESH:D005357] (737)  Bone Diseases, Endocrine [MESH:D001849] (747)   Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 2 [MESH:C563172] (35)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Spinal Diseases [MESH:D013122] (2485)   Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Kleefstra Syndrome [MESH:C563043] (25)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Silver-Russell Syndrome [MESH:D056730] (142)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Microcephaly [MESH:D008831] (700)   Seckel syndrome 1 [MESH:C537533] (63)  Limb Deformities, Congenital [MESH:D017880] (1813)   Polydactyly [MESH:D017689] (318)   Hydrolethalus Syndrome 1 [MESH:C565504] (14)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)  Digestive System Neoplasms [MESH:D004067] (7493)   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)   Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Esophageal Stenosis [MESH:D004940] (490)  Esophagitis [MESH:D004941] (1120)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Gastroenteritis [MESH:D005759] (4066)   Colitis [MESH:D003092] (3199)  Esophagitis [MESH:D004941] (1120)  Inflammatory Bowel Diseases [MESH:D015212] (3492)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  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)   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)   Inflammatory Bowel Diseases [MESH:D015212] (3492)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Malabsorption Syndromes [MESH:D008286] (492)   Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Cholestasis, Intrahepatic [MESH:D002780] (1510)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Fatty Liver [MESH:D005234] (3584)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  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 Palate [MESH:D002972] (1330) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Respiratory System Abnormalities [MESH:D015619] (243)  Thoracic Diseases [MESH:D013896] (81)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Lung Diseases [MESH:D008171] (7249)   Hypertension, Pulmonary [MESH:D006976] (2000)  Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Alveolitis, Extrinsic Allergic [MESH:D000542] (496)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  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)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Chudley-Mccullough syndrome [MESH:C535459] (45)  MYH9-Related Disorders [MESH:C535507] (46)  Macrothrombocytopenia progressive deafness [MESH:C537831] (46)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Deafness, Autosomal Recessive 28 [MESH:C565218] (26)  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)   Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Familial porencephaly [MESH:C536850] (77)  Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia 6, torsion [MESH:C538003] (13)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  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)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Lewy Body Disease [MESH:D020961] (1143)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)   Frontotemporal Dementia [MESH:D057180] (300)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Hydrocephalus [MESH:D006849] (276)   Hydrolethalus Syndrome 1 [MESH:C565504] (14)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Pituitary Neoplasms [MESH:D010911] (981)  Hypopituitarism [MESH:D007018] (732)   Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 2 [MESH:C563172] (35)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)   Hydrolethalus Syndrome 1 [MESH:C565504] (14)  Leukoencephalopathies [MESH:D056784] (1916)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Movement Disorders [MESH:D009069] (4823)   Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Dystonic Disorders [MESH:D020821] (729)   Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia 6, torsion [MESH:C538003] (13)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Spinal Cord Diseases [MESH:D013118] (4376)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 2, Juvenile [MESH:C565957] (29)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Demyelinating Diseases [MESH:D003711] (2917)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Hereditary spastic paralysis, infantile onset ascending [MESH:C537217] (29)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Seckel syndrome 1 [MESH:C537533] (63)  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)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia 6, torsion [MESH:C538003] (13)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Hereditary spastic paralysis, infantile onset ascending [MESH:C537217] (29)  Motor Neuron Disease [MESH:D016472] (3670)   Primary lateral sclerosis juvenile [MESH:C536416] (29)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 2, Juvenile [MESH:C565957] (29)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 2, Juvenile [MESH:C565957] (29)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Neurologic Manifestations [MESH:D009461] (8964)   Pain [MESH:D010146] (3875)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Memory Disorders [MESH:D008569] (3233)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Intellectual Disability [MESH:D008607] (3054)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Kleefstra Syndrome [MESH:C563043] (25)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Chromosome Xp11.3 Deletion Syndrome [MESH:C564481] (6)  Adrenoleukodystrophy [MESH:D000326] (1348)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Muscle Hypotonia [MESH:D009123] (258)   Three M Syndrome 2 [MESH:C567862] (22)  Paralysis [MESH:D010243] (2043)   Hemiplegia [MESH:D006429] (184)   Familial porencephaly [MESH:C536850] (77)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Chudley-Mccullough syndrome [MESH:C535459] (45)  MYH9-Related Disorders [MESH:C535507] (46)  Macrothrombocytopenia progressive deafness [MESH:C537831] (46)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Deafness, Autosomal Recessive 28 [MESH:C565218] (26)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Primary lateral sclerosis juvenile [MESH:C536416] (29)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 2, Juvenile [MESH:C565957] (29)  Muscular Diseases [MESH:D009135] (3538)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Hereditary spastic paralysis, infantile onset ascending [MESH:C537217] (29)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eye Abnormalities [MESH:D005124] (1233)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Doyne honeycomb retinal dystrophy [MESH:C535602] (44)  Sveinsson Chorioretinal Atrophy [MESH:C566236] (22)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Doyne honeycomb retinal dystrophy [MESH:C535602] (44)  Sveinsson Chorioretinal Atrophy [MESH:C566236] (22)  Retinitis Pigmentosa [MESH:D012174] (414)   Chromosome Xp11.3 Deletion Syndrome [MESH:C564481] (6)  Retinitis Pigmentosa 2 [MESH:C567523] (6)  Eye Hemorrhage [MESH:D005130] (94)   Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinal Degeneration [MESH:D012162] (2386)   Sveinsson Chorioretinal Atrophy [MESH:C566236] (22)  Macular Degeneration [MESH:D008268] (995)   Macular Edema [MESH:D008269] (557)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Chromosome Xp11.3 Deletion Syndrome [MESH:C564481] (6)  Retinitis Pigmentosa 2 [MESH:C567523] (6)  Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)  Penile Neoplasms [MESH:D010412] (890)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)  Urogenital Abnormalities [MESH:D014564] (2065)   Cryptorchidism [MESH:D003456] (215)  Hypospadias [MESH:D007021] (798)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Renal [MESH:D006977] (698)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Uterine Diseases [MESH:D014591] (2479)   Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Abnormalities [MESH:D014564] (2043)   Hypospadias [MESH:D007021] (798)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Renal [MESH:D006977] (698)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Placenta Diseases [MESH:D010922] (1781)  Polyhydramnios [MESH:D006831] (123)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Cardiovascular Diseases [MESH:D002318] (10123)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Kleefstra Syndrome [MESH:C563043] (25)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathies [MESH:D009202] (5331)   Alpha-B Crystallinopathy [MESH:C563848] (135)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Heart Defects, Congenital [MESH:D006330] (2443)   Kleefstra Syndrome [MESH:C563043] (25)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Retinal Vein Occlusion [MESH:D012170] (607)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Hypertension [MESH:D006973] (5655)   Hypertension, Renal [MESH:D006977] (698)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Raynaud Disease [MESH:D011928] (490)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Anemia [MESH:D000740] (3966)   Anemia, Sideroblastic [MESH:D000756] (636)  Anemia, Hemolytic [MESH:D000743] (3083)   Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Blood Coagulation Disorders [MESH:D001778] (1828)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   MYH9-Related Disorders [MESH:C535507] (46)  Macrothrombocytopenia progressive deafness [MESH:C537831] (46)  Thrombotic Microangiopathies [MESH:D057049] (2598)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative [MESH:D054438] (18)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Anemia, Sideroblastic [MESH:D000756] (636)  Myeloproliferative Disorders [MESH:D009196] (1492)   Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemoglobinopathies [MESH:D006453] (1863)   Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Hemorrhagic Disorders [MESH:D006474] (3359)   Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328)  Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphoproliferative Disorders [MESH:D008232] (4638)   Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) 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)  Eye Abnormalities [MESH:D005124] (1233)  Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Silver-Russell Syndrome [MESH:D056730] (142)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Kleefstra Syndrome [MESH:C563043] (25)  Chromosome Disorders [MESH:D025063] (2030)   Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Silver-Russell Syndrome [MESH:D056730] (142)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Kleefstra Syndrome [MESH:C563043] (25)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Microcephaly [MESH:D008831] (700)   Seckel syndrome 1 [MESH:C537533] (63)  Limb Deformities, Congenital [MESH:D017880] (1813)   Hand Deformities, Congenital [MESH:D006228] (587)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Polydactyly [MESH:D017689] (318)   Hydrolethalus Syndrome 1 [MESH:C565504] (14)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Hereditary spastic paralysis, infantile onset ascending [MESH:C537217] (29)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Seckel syndrome 1 [MESH:C537533] (63)  Skin Abnormalities [MESH:D012868] (1723)   Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  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 Palate [MESH:D002972] (1330)  Urogenital Abnormalities [MESH:D014564] (2064)   Cryptorchidism [MESH:D003456] (215)  Hypospadias [MESH:D007021] (798)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Loeys-Dietz Syndrome [MESH:D055947] (263)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Chromosome Disorders [MESH:D025063] (2030)   Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Silver-Russell Syndrome [MESH:D056730] (142)  Dwarfism [MESH:D004392] (783)   Seckel syndrome 1 [MESH:C537533] (63)  Three M Syndrome 2 [MESH:C567862] (22)  Silver-Russell Syndrome [MESH:D056730] (142)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Doyne honeycomb retinal dystrophy [MESH:C535602] (44)  Sveinsson Chorioretinal Atrophy [MESH:C566236] (22)  Retinitis Pigmentosa [MESH:D012174] (442)   Chromosome Xp11.3 Deletion Syndrome [MESH:C564481] (6)  Retinitis Pigmentosa 2 [MESH:C567523] (6)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Chromosome Xp11.3 Deletion Syndrome [MESH:C564481] (6)  Adrenoleukodystrophy [MESH:D000326] (1348)  Hemoglobinopathies [MESH:D006453] (1863)   Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia 6, torsion [MESH:C538003] (13)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Hereditary spastic paralysis, infantile onset ascending [MESH:C537217] (29)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Chromosome Xp11.3 Deletion Syndrome [MESH:C564481] (6)  Adrenoleukodystrophy [MESH:D000326] (1348)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Adrenoleukodystrophy [MESH:D000326] (1348)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Wilms Tumor [MESH:D009396] (553)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Skin Diseases, Genetic [MESH:D012873] (3456)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Dermatitis, Atopic [MESH:D003876] (2052)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Diabetes Mellitus, Transient Neonatal, 1 [MESH:C563322] (58)  Asphyxia Neonatorum [MESH:D001238] (1648)  Ichthyosis [MESH:D007057] (476)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Hair Diseases [MESH:D006201] (1891)  Pruritus [MESH:D011537] (647)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Keratosis [MESH:D007642] (1941)   Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Skin Abnormalities [MESH:D012868] (1709)   Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Ichthyosis [MESH:D007057] (481)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  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)   Keratosis Follicularis Spinulosa Decalvans, X-Linked [MESH:C536159] (78)  Dermatitis, Atopic [MESH:D003876] (2052)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 2 [MESH:C536195] (55)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Partial, Acquired [MESH:C562448] (26)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Iron Metabolism Disorders [MESH:D019189] (2139)  Metabolic Syndrome X [MESH:D024821] (2151)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Li-Fraumeni Syndrome [MESH:D016864] (859)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Hypoglycemia [MESH:D007003] (2420)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Transient Neonatal, 1 [MESH:C563322] (58)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipidoses [MESH:D008064] (1655)  Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Partial, Acquired [MESH:C562448] (26)  Malabsorption Syndromes [MESH:D008286] (1869)   Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pelizaeus-Merzbacher Disease [MESH:D020371] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Adrenoleukodystrophy [MESH:D000326] (1348)  Mitochondrial Diseases [MESH:D028361] (2561)   Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)  Proteostasis Deficiencies [MESH:D057165] (3522)   TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 2, Juvenile [MESH:C565957] (29)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Partial, Acquired [MESH:C562448] (26)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Bone Diseases, Endocrine [MESH:D001849] (173)  Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Transient Neonatal, 1 [MESH:C563322] (58)  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 Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Dwarfism [MESH:D004392] (698)   Seckel syndrome 1 [MESH:C537533] (63)  Three M Syndrome 2 [MESH:C567862] (22)  Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 2 [MESH:C563172] (35)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Gonadal Disorders [MESH:D006058] (5088)   Hypogonadism [MESH:D007006] (1123)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Cryptorchidism [MESH:D003456] (215)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Neoplasms [MESH:D010911] (981)  Hypopituitarism [MESH:D007018] (732)   Dwarfism, Pituitary [MESH:D004393] (235)   Pituitary Hormone Deficiency, Combined, 2 [MESH:C563172] (35)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroiditis [MESH:D013966] (158)   Thyroiditis, Autoimmune [MESH:D013967] (149)   Hashimoto Disease [MESH:D050031] (98) C20. Immune System Diseases  C20. Immune System Diseases  Z. Exceptions (350)   Not Fully Specified [NFS] (350)  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Hypersensitivity [MESH:D006967] (5873)   Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (3914)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Atrophy [MESH:D001284] (2603)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Nails, Malformed [MESH:D009264] (184)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Pathologic Processes [MESH:D010335] (9863)   Emphysema [MESH:D004646] (1096)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Chromosome Aberrations [MESH:D002869] (2352)   Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Kleefstra Syndrome [MESH:C563043] (25)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Granuloma [MESH:D006099] (587)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Growth Disorders [MESH:D006130] (2438)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Eye Hemorrhage [MESH:D005130] (94)   Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Inflammation [MESH:D007249] (5241)   Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Signs and Symptoms [MESH:D012816] (10659)   Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Reticulocytosis [MESH:D045262] (514)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Pain [MESH:D010146] (3869)  Seizures [MESH:D012640] (4502)  Dyskinesias [MESH:D020820] (3285)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Memory Disorders [MESH:D008569] (3233)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Intellectual Disability [MESH:D008607] (1476)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Kleefstra Syndrome [MESH:C563043] (25)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Muscle Hypotonia [MESH:D009123] (258)   Three M Syndrome 2 [MESH:C567862] (22)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Hemiplegia [MESH:D006429] (184)   Familial porencephaly [MESH:C536850] (77)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Chudley-Mccullough syndrome [MESH:C535459] (45)  MYH9-Related Disorders [MESH:C535507] (46)  Macrothrombocytopenia progressive deafness [MESH:C537831] (46)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Deafness, Autosomal Recessive 28 [MESH:C565218] (26)  Pain [MESH:D010146] (4511)   Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Skin Manifestations [MESH:D012877] (1250)   Pruritus [MESH:D011537] (648)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293) 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)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Fractures, Bone [MESH:D050723] (597)  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)  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) D01. Inorganic Chemicals  D01. Inorganic Chemicals  Elements [MESH:D004602] (999)   Metals, Heavy [MESH:D019216] (597)   Copper [MESH:D003300] (60)  Transition Elements [MESH:D028561] (454)   Copper [MESH:D003300] (60)  Metals [MESH:D008670] (894)   Metals, Heavy [MESH:D019216] (597)   Copper [MESH:D003300] (60) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Kleefstra Syndrome [MESH:C563043] (25)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Kleefstra Syndrome [MESH:C563043] (25) 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)  Kleefstra Syndrome [MESH:C563043] (25)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 6-12 and X [MESH:D002906] (120)   Chromosomes, Human, Pair 9 [MESH:D002899] (40)   Kleefstra Syndrome [MESH:C563043] (25)  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)  Kleefstra Syndrome [MESH:C563043] (25)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Kleefstra Syndrome [MESH:C563043] (25)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Kleefstra Syndrome [MESH:C563043] (25)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Kleefstra Syndrome [MESH:C563043] (25)