Item 6 of 39 (back to results) previous next   docetaxel C067311               MeSH Unique Identifier: C067311 Scope Notes: Semisynthetic analog of taxol Chemical – Gene Interaction Note 1: [docetaxel results in decreased susceptibility to docetaxel] which results in increased expression of ABCA1 mRNA Note 2: [docetaxel results in decreased susceptibility to docetaxel] which results in increased expression of ABCA10 mRNA Click here for more information

Current search: C08. Respiratory Tract Diseases: Respiratory Tract Diseases [MESH:D012140] > Pleural Diseases [MESH:D010995] > Pleural Effusion [MESH:D010996] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily A [HGNC:ABCA] (29)   ATP-binding cassette, sub-family A (ABC1), member 06 [HGNC:ABCA6] (13)  ATP-binding cassette, sub-family A (ABC1), member 07 [HGNC:ABCA7] (7)  ATP-binding cassette, sub-family A (ABC1), member 12 [HGNC:ABCA12] (14)  ATP-binding cassette transporters, subfamily B [HGNC:ABCB] (452)   ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355)  ATP-binding cassette, sub-family B (MDR/TAP), member 04 [HGNC:ABCB4] (30)  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 2 [HGNC:ABCC2] (152)  ATP-binding cassette, sub-family C (CFTR/MRP), member 3 [HGNC:ABCC3] (89)  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)  ATP-binding cassette, sub-family C (CFTR/MRP), member 9 [HGNC:ABCC9] (9)  ATP-binding cassette transporters, subfamily G [HGNC:ABCG] (184)   ATP-binding cassette, sub-family G (WHITE), member 2 [HGNC:ABCG2] (147)  Basic leucine zipper proteins [HGNC:bZIP] (670)   jun proto-oncogene [HGNC:JUN] (290)  CD molecules [HGNC:CD] (1459)   ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355)  ATP-binding cassette, sub-family G (WHITE), member 2 [HGNC:ABCG2] (147)  melanoma cell adhesion molecule [HGNC:MCAM] (21)  tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155)  tumor necrosis factor receptor superfamily, member 10a [HGNC:TNFRSF10A] (70)  tumor necrosis factor receptor superfamily, member 10b [HGNC:TNFRSF10B] (124)  v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2 [HGNC:ERBB2] (109)  Cyclin-dependent kinases [HGNC:CDK] (338)   cyclin-dependent kinase 01 [HGNC:CDK1] (151)  cyclin-dependent kinase 02 [HGNC:CDK2] (177)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 01, subfamily B, polypeptide 01 [HGNC:CYP1B1] (301)  cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612)  cytochrome P450, family 19, subfamily A, polypeptide 01 [HGNC:CYP19A1] (210)  Glutathione S-transferases [HGNC:GST] (460)   Glutathione S-transferases, soluble [HGNC:SGST] (447)   glutathione S-transferase pi 1 [HGNC:GSTP1] (218)  Histones [HGNC:HIST] (173)   Histones, Replication-independent [HGNC:RIH] (148)   H2A histone family, member X [HGNC:H2AFX] (129)  Immunoglobulin superfamily domain containing [HGNC:IGSF] (761)   V-set domain containing [HGNC:VSET] (188)   melanoma cell adhesion molecule [HGNC:MCAM] (21)  C2-set domain containing [HGNC:C2SET] (225)   melanoma cell adhesion molecule [HGNC:MCAM] (21)  Immunoglobulin-like domain containing [HGNC:IGD] (645)   melanoma cell adhesion molecule [HGNC:MCAM] (21)  Interferons and interferon receptors [HGNC:IFN] (684)   interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)  Intermediate filaments [HGNC:IF] (273)   Type I. Keratins (acidic) [HGNC:] (120)   keratin 18 [HGNC:KRT18] (50)  Keratins [HGNC:KRT] (161)   keratin 18 [HGNC:KRT18] (50)  Kinesins [HGNC:KIF] (68)   kinesin family member 05A [HGNC:KIF5A] (3)  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)   nuclear receptor subfamily 1, group I, member 2 [HGNC:NR1I2] (328)  progesterone receptor [HGNC:PGR] (209)  Protease activated receptors [HGNC:F2R] (81)   coagulation factor II (thrombin) receptor [HGNC:F2R] (49)  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)  Regulators of G-protein signaling [HGNC:RGS] (98)   regulator of G-protein signaling 17 [HGNC:RGS17] (12)  RING-type zinc fingers [HGNC:RNF] (151)   checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase [HGNC:CHFR] (11)  Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898)   tumor necrosis factor [HGNC:TNF] (795)  tumor necrosis factor (ligand) superfamily, member 10 [HGNC:TNFSF10] (155)  Tumor necrosis factor receptor superfamily [HGNC:TNFRSF] (295)   tumor necrosis factor receptor superfamily, member 10a [HGNC:TNFRSF10A] (70)  tumor necrosis factor receptor superfamily, member 10b [HGNC:TNFRSF10B] (124) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  cotreatment (1499)  expression (494)  folding (77)  localization (731)  reaction (624)  response to substance (623)  transport (172)  Decreases (5154)   activity (2549)  expression (2187)  localization (74)  phosphorylation (590)  reaction (3393)  response to substance (713)  secretion (346)  ubiquitination (21)  Increases (5571)   activity (2865)  cleavage (666)  degradation (347)  expression (3238)  metabolic processing (740)  phosphorylation (1060)  reaction (1574)  response to substance (641)  secretion (901)  ubiquitination (61) A. Anatomy  A. Anatomy  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Skull [MESH:D012886] (610)   Facial Bones [MESH:D005147] (539)   Jaw [MESH:D007568] (524)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Sense Organs [MESH:D012679] (1060)   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)  Stomatognathic System [MESH:D013284] (673)   Jaw [MESH:D007568] (528)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  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)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Skin Diseases, Infectious [MESH:D012874] (415)   Paronychia [MESH:D010304] (6) 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)   Papillomavirus Infections [MESH:D030361] (630)  Herpesviridae Infections [MESH:D006566] (1944)   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)   Papillomavirus Infections [MESH:D030361] (537) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Protozoan Infections [MESH:D011528] (3014)   Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Malaria [MESH:D008288] (2175)   Malaria, Falciparum [MESH:D016778] (438)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Hormone-Dependent [MESH:D009376] (20)  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, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Erythroblastic, Acute [MESH:D004915] (89)  Leukemia, Megakaryoblastic, Acute [MESH:D007947] (279)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Chondroma [MESH:D002812] (155)  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)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyosarcoma [MESH:D007890] (977)  Myoma [MESH:D009214] (203)   Rhabdomyoma [MESH:D012207] (200)  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)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Experimental [MESH:D012513] (128)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  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)   Germinoma [MESH:D018237] (201)   Seminoma [MESH:D018239] (195)  Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  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)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   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)  Adenocarcinoma, Mucinous [MESH:D002288] (8)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Endometrioid [MESH:D018269] (15)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Cystic, Mucinous, and Serous [MESH:D018297] (30)   Adenocarcinoma, Mucinous [MESH:D002288] (8)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  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)  Nerve Sheath Neoplasms [MESH:D018317] (365)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  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)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangioma [MESH:D006391] (690)  Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Nevus [MESH:D009506] (340)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  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)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Eye Neoplasms [MESH:D005134] (400)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  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)  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)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  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)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Thoracic Neoplasms [MESH:D013899] (6032)   Thymus Neoplasms [MESH:D013953] (247)  Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Endometrial Neoplasms [MESH:D016889] (1987)   Carcinoma, Endometrioid [MESH:D018269] (15)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Phyllodes Tumor of the Prostate [MESH:C549759] (110)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Sarcoma, Experimental [MESH:D012513] (128)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Paraneoplastic Syndromes [MESH:D010257] (231)   Paraneoplastic Endocrine Syndromes [MESH:D009384] (207)   ACTH Syndrome, Ectopic [MESH:D000182] (200)  Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Precancerous Conditions [MESH:D011230] (2858)   Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921) 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)   Marfan Syndrome [MESH:D008382] (646)  Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Osteochondrodysplasias [MESH:D010009] (2440)   Cantu syndrome [MESH:C535572] (42)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Enchondromatosis [MESH:D004687] (170)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)   Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Osteonecrosis [MESH:D010020] (539)   Femur Head Necrosis [MESH:D005271] (268)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)   Intervertebral disc disease [MESH:C535531] (514)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  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)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Joint Diseases [MESH:D007592] (4657)   Arthralgia [MESH:D018771] (191)  Synovitis [MESH:D013585] (270)  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)  Chondrocalcinosis [MESH:D002805] (213)  Osteoarthritis [MESH:D010003] (1743)  Sacroiliitis [MESH:D058566] (202)  Gout [MESH:D006073] (261)   Arthritis, Gouty [MESH:D015210] (211)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Muscle Weakness [MESH:D018908] (478)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   Mitochondrial neurogastrointestinal encephalopathy syndrome [MESH:C537477] (71)  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)   Costello Syndrome [MESH:D056685] (407)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Microcephaly [MESH:D008831] (700)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Limb Deformities, Congenital [MESH:D017880] (1813)   Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Gout [MESH:D006073] (261)   Arthritis, Gouty [MESH:D015210] (211) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Bile Duct Neoplasms [MESH:D001650] (367)  Cholangitis [MESH:D002761] (203)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Cholestasis, progressive familial intrahepatic 3 [MESH:C535935] (101)  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)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophagitis [MESH:D004941] (1120)  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)  Gastroenteritis [MESH:D005759] (4066)   Esophagitis [MESH:D004941] (1120)  Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   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)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  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 Obstruction [MESH:D007415] (146)   Ileus [MESH:D045823] (128)   Intestinal Pseudo-Obstruction [MESH:D007418] (118)   Mitochondrial neurogastrointestinal encephalopathy syndrome [MESH:C537477] (71)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  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)  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)  Hypertension, Portal [MESH:D006975] (869)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Cholestasis, progressive familial intrahepatic 3 [MESH:C535935] (101)  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)   End Stage Liver Disease [MESH:D058625] (108)  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)   Cirrhosis, Familial [MESH:C566123] (179)  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)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  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)  Periapical Diseases [MESH:D010483] (186)   Periapical Periodontitis [MESH:D010485] (183)  Mouth Diseases [MESH:D009059] (4783)   Facial Paralysis [MESH:D005158] (238)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Stomatitis [MESH:D013280] (1235)  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)  Tongue Neoplasms [MESH:D014062] (1518)  Periodontal Diseases [MESH:D010510] (1001)   Periapical Diseases [MESH:D010483] (186)   Periapical Periodontitis [MESH:D010485] (183)  Periodontitis [MESH:D010518] (843)   Periapical Periodontitis [MESH:D010485] (183)  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)  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)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Surfactant Metabolism Dysfunction, Pulmonary, 3 [MESH:C567046] (24)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  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)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pulmonary Alveolar Proteinosis [MESH:D011649] (139)   Surfactant Metabolism Dysfunction, Pulmonary, 3 [MESH:C567046] (24)  Pleural Diseases [MESH:D010995] (2240)   Pleural Effusion [MESH:D010996] (39)  Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Dyspnea [MESH:D004417] (248)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  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)  Pneumonia [MESH:D011014] (3482)  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)   Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  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)  Restless Legs Syndrome [MESH:D012148] (379)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)   Hypotension, Orthostatic [MESH:D007024] (679)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Brain Damage, Chronic [MESH:D001925] (311)   Cerebral Palsy [MESH:D002547] (300)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Mitochondrial Encephalomyopathies [MESH:D017237] (158)   Mitochondrial neurogastrointestinal encephalopathy syndrome [MESH:C537477] (71)  Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  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)  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)  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)  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)  Spasms, Infantile [MESH:D013036] (468)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Hypopituitarism [MESH:D007018] (732)  Inappropriate ADH Syndrome [MESH:D007177] (178)  Hyperpituitarism [MESH:D006964] (1250)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  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)   Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Ocular Motility Disorders [MESH:D015835] (364)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  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)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2I [MESH:C535416] (22)  Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)  Charcot-Marie-Tooth Disease, Dominant Intermediate D [MESH:C564333] (22)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Nervous System Neoplasms [MESH:D009423] (3073)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  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)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Peripheral Nervous System Neoplasms [MESH:D010524] (287)   Nerve Sheath Neoplasms [MESH:D018317] (286)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neurodegenerative Diseases [MESH:D019636] (6613)   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)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2I [MESH:C535416] (22)  Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)  Charcot-Marie-Tooth Disease, Dominant Intermediate D [MESH:C564333] (22)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  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)  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)  Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)  Reflex, Abnormal [MESH:D012021] (485)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)  Gait Ataxia [MESH:D020234] (26)  Myoclonus [MESH:D009207] (427)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Gait Disorders, Neurologic [MESH:D020233] (491)   Gait Ataxia [MESH:D020234] (26)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Consciousness Disorders [MESH:D003244] (680)  Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Facial Paralysis [MESH:D005158] (238)  Quadriplegia [MESH:D011782] (115)  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)   Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Taste Disorders [MESH:D013651] (461)   Dysgeusia [MESH:D004408] (24)  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)   Mitochondrial neurogastrointestinal encephalopathy syndrome [MESH:C537477] (71)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Peripheral Nervous System Neoplasms [MESH:D010524] (287)   Nerve Sheath Neoplasms [MESH:D018317] (286)  Polyneuropathies [MESH:D011115] (1134)   Tangier Disease [MESH:D013631] (170)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2I [MESH:C535416] (22)  Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)  Charcot-Marie-Tooth Disease, Dominant Intermediate D [MESH:C564333] (22)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Restless Legs Syndrome [MESH:D012148] (379)  Parasomnias [MESH:D020447] (453)   Restless Legs Syndrome [MESH:D012148] (379)  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  Z. Exceptions (245)   Not Fully Specified [NFS] (245)  Eye Diseases [MESH:D005128] (6245)   Eyelid Diseases [MESH:D005141] (882)  Conjunctival Diseases [MESH:D003229] (273)   Conjunctivitis [MESH:D003231] (133)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  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)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Cone-Rod Dystrophy 3 [MESH:C565827] (9)  Retinitis Pigmentosa 19 [MESH:C566637] (9)  Eye Manifestations [MESH:D005132] (208)   Eye Pain [MESH:D058447] (207)  Eye Neoplasms [MESH:D005134] (413)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  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)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Stargardt disease 1 [MESH:C535804] (15)  Macular Degeneration, Age-Related, 2 [MESH:C562479] (9)  Macular Edema [MESH:D008269] (557)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Cone-Rod Dystrophy 3 [MESH:C565827] (9)  Retinitis Pigmentosa 19 [MESH:C566637] (9)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550) 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)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Aromatase deficiency [MESH:C537436] (277)  Azoospermia [MESH:D053713] (1052)  Penile Diseases [MESH:D010409] (1805)   Penile Neoplasms [MESH:D010412] (890)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)   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)  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)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Diabetes Insipidus [MESH:D003919] (354)  Diabetic Nephropathies [MESH:D003928] (2301)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Nephrocalcinosis [MESH:D009397] (311)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Lupus Nephritis [MESH:D008181] (602)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4374)   Cystitis [MESH:D003556] (604)  Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Hematuria [MESH:D006417] (477)  Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Carcinoma, Endometrioid [MESH:D018269] (15)  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)  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)   Carcinoma, Endometrioid [MESH:D018269] (15)  Uterine Neoplasms [MESH:D014594] (2433)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Endometrial Neoplasms [MESH:D016889] (1989)   Carcinoma, Endometrioid [MESH:D018269] (15)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Diabetes Insipidus [MESH:D003919] (354)  Diabetic Nephropathies [MESH:D003928] (2301)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Nephrocalcinosis [MESH:D009397] (311)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Lupus Nephritis [MESH:D008181] (602)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4375)   Cystitis [MESH:D003556] (604)  Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Hematuria [MESH:D006417] (477)  Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Pregnancy Complications [MESH:D011248] (4768)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Placenta Diseases [MESH:D010922] (1781)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Marfan Syndrome [MESH:D008382] (646)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  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)   Cardiac Output, High [MESH:D016534] (123)  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)  Long QT Syndrome [MESH:D008133] (693)  Ventricular Fibrillation [MESH:D014693] (624)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Heart Block [MESH:D006327] (571)   Sick Sinus Syndrome [MESH:D012804] (293)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Cardiomegaly [MESH:D006332] (4081)   Cantu syndrome [MESH:C535572] (42)  Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1o [MESH:C563906] (42)  Cardiomyopathies [MESH:D009202] (5331)   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)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1o [MESH:C563906] (42)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Marfan Syndrome [MESH:D008382] (646)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Shock, Cardiogenic [MESH:D012770] (269)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Ventricular Dysfunction, Right [MESH:D018497] (113)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (203)  Vascular Diseases [MESH:D014652] (8691)   Hyperemia [MESH:D006940] (2372)  Hypertension [MESH:D006973] (5655)  Retinal Vein Occlusion [MESH:D012170] (607)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Aortic Diseases [MESH:D001018] (1737)   Aortitis [MESH:D001025] (4)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Coronary Artery Disease [MESH:D003324] (2685)  Atherosclerosis [MESH:D050197] (4188)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  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)   Ischemic Attack, Transient [MESH:D002546] (1313)  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)  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)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Thrombosis [MESH:D013927] (3101)   Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Thrombophlebitis [MESH:D013924] (67)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  Shock, Cardiogenic [MESH:D012770] (269)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Phlebitis [MESH:D010689] (115)   Thrombophlebitis [MESH:D013924] (67)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Aortitis [MESH:D001025] (4)  Phlebitis [MESH:D010689] (114)   Thrombophlebitis [MESH:D013924] (67) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Z. Exceptions (453)   Not Fully Specified [NFS] (453)  Hematologic Diseases [MESH:D006402] (6174)   Pancytopenia [MESH:D010198] (332)  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)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Spherocytosis, Hereditary [MESH:D013103] (137)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  Hemoglobinuria, Paroxysmal [MESH:D006457] (293)   Bone Marrow failure syndromes [MESH:C536572] (248)  Blood Coagulation Disorders [MESH:D001778] (1828)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  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-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Hemoglobinuria, Paroxysmal [MESH:D006457] (293)   Bone Marrow failure syndromes [MESH:C536572] (248)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Erythroblastic, Acute [MESH:D004915] (89)  Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  Hemorrhagic Disorders [MESH:D006474] (3359)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Leukocyte Disorders [MESH:D007960] (2662)   Leukocytosis [MESH:D007964] (988)  Leukostasis [MESH:D018921] (769)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Lymphatic Diseases [MESH:D008206] (5167)   Thymus Neoplasms [MESH:D013953] (247)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  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)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Splenic Diseases [MESH:D013158] (1323)   Hypersplenism [MESH:D006971] (341) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Multiple [MESH:D000015] (3192)   Costello Syndrome [MESH:D056685] (407)  Marfan Syndrome [MESH:D008382] (646)  Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Long QT Syndrome [MESH:D008133] (693)  Marfan Syndrome [MESH:D008382] (646)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  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)  Eye Abnormalities [MESH:D005124] (1233)   Peters anomaly [MESH:C537884] (465)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Microcephaly [MESH:D008831] (700)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Limb Deformities, Congenital [MESH:D017880] (1813)   Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  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)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2I [MESH:C535416] (22)  Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)  Charcot-Marie-Tooth Disease, Dominant Intermediate D [MESH:C564333] (22)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Skin Abnormalities [MESH:D012868] (1723)   Pseudoxanthoma Elasticum [MESH:D011561] (115)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Lamellar ichthyosis, type 2 [MESH:C537264] (16)  Harlequin type ichthyosis [MESH:C538424] (16)  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)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Cirrhosis, Familial [MESH:C566123] (179)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Costello Syndrome [MESH:D056685] (407)  Marfan Syndrome [MESH:D008382] (646)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Spherocytosis, Hereditary [MESH:D013103] (137)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Chromosome Disorders [MESH:D025063] (2030)   Mosaic variegated aneuploidy syndrome [MESH:C536987] (95)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Cone-Rod Dystrophy 3 [MESH:C565827] (9)  Retinitis Pigmentosa 19 [MESH:C566637] (9)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Cantu syndrome [MESH:C535572] (42)  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)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2I [MESH:C535416] (22)  Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)  Charcot-Marie-Tooth Disease, Dominant Intermediate D [MESH:C564333] (22)  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  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)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Aromatase deficiency [MESH:C537436] (277)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Hyperhomocysteinemia [MESH:D020138] (1724)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease XII [MESH:C562718] (98)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   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)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Oroticaciduria 1 [MESH:C537136] (41)  Dihydropyrimidine Dehydrogenase Deficiency [MESH:D054067] (88)  Gout [MESH:D006073] (261)   Arthritis, Gouty [MESH:D015210] (211)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Lamellar ichthyosis, type 2 [MESH:C537264] (16)  Harlequin type ichthyosis [MESH:C538424] (16)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Jaundice, Neonatal [MESH:D007567] (290)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Ichthyosis [MESH:D007057] (476)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Lamellar ichthyosis, type 2 [MESH:C537264] (16)  Harlequin type ichthyosis [MESH:C538424] (16)  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)  Marfan Syndrome [MESH:D008382] (646)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Scleroderma, Localized [MESH:D012594] (1597)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Erythema [MESH:D004890] (1330)  Hand Dermatoses [MESH:D006229] (25)  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)  Gynecomastia [MESH:D006177] (484)   Aromatase deficiency [MESH:C537436] (277)  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)   Hand-Foot Syndrome [MESH:D060831] (4)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Foot Diseases [MESH:D005534] (31)   Foot Dermatoses [MESH:D005533] (18)  Hair Diseases [MESH:D006201] (1891)   Hirsutism [MESH:D006628] (323)  Hypertrichosis [MESH:D006983] (97)   Cantu syndrome [MESH:C535572] (42)  Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)  Keratosis [MESH:D007642] (1941)   Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Lamellar ichthyosis, type 2 [MESH:C537264] (16)  Harlequin type ichthyosis [MESH:C538424] (16)  Nail Diseases [MESH:D009260] (203)   Paronychia [MESH:D010304] (6)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Skin Abnormalities [MESH:D012868] (1709)   Pseudoxanthoma Elasticum [MESH:D011561] (115)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Lamellar ichthyosis, type 2 [MESH:C537264] (16)  Harlequin type ichthyosis [MESH:C538424] (16)  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)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Lamellar ichthyosis, type 2 [MESH:C537264] (16)  Harlequin type ichthyosis [MESH:C538424] (16)  Skin Diseases, Infectious [MESH:D012874] (2684)   Paronychia [MESH:D010304] (6)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  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)   Urticaria [MESH:D014581] (2668) 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)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Mitochondrial Encephalomyopathies [MESH:D017237] (158)   Mitochondrial neurogastrointestinal encephalopathy syndrome [MESH:C537477] (71)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Hypocalcemia [MESH:D006996] (378)  Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  Nephrocalcinosis [MESH:D009397] (311)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Fanconi Anemia [MESH:D005199] (1604)  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, Experimental [MESH:D003921] (4771)  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)  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)  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)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Aromatase deficiency [MESH:C537436] (277)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Hyperhomocysteinemia [MESH:D020138] (1724)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease XII [MESH:C562718] (98)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   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)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Oroticaciduria 1 [MESH:C537136] (41)  Dihydropyrimidine Dehydrogenase Deficiency [MESH:D054067] (88)  Gout [MESH:D006073] (261)   Arthritis, Gouty [MESH:D015210] (211)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Mitochondrial Diseases [MESH:D028361] (2561)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   Mitochondrial neurogastrointestinal encephalopathy syndrome [MESH:C537477] (71)  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)  Proteostasis Deficiencies [MESH:D057165] (3522)   TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hypernatremia [MESH:D006955] (215)  Hypocalcemia [MESH:D006996] (368)  Hypokalemia [MESH:D007008] (1041)  Inappropriate ADH Syndrome [MESH:D007177] (178)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   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)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  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 Hyperplasia, Congenital [MESH:D000312] (674)  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)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Cushing Syndrome [MESH:D003480] (282)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  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)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   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)  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)   Carcinoma, Endometrioid [MESH:D018269] (15)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Pituitary Diseases [MESH:D010900] (1829)   Diabetes Insipidus [MESH:D003919] (302)  Hypopituitarism [MESH:D007018] (732)  Inappropriate ADH Syndrome [MESH:D007177] (178)  Hyperpituitarism [MESH:D006964] (1259)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040) 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, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2695)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Anaphylaxis [MESH:D000707] (299)  Asthma, Aspirin-Induced [MESH:D055963] (1055)  Dermatitis, Atopic [MESH:D003876] (2052)  Urticaria [MESH:D014581] (2668)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   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)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  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)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, AIDS-Related [MESH:D016483] (278)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Plaque, Atherosclerotic [MESH:D058226] (696)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)   Cantu syndrome [MESH:C535572] (42)  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)   Death [MESH:D003643] (1328)  Emphysema [MESH:D004646] (1096)  Fibrosis [MESH:D005355] (3133)  Gliosis [MESH:D005911] (1419)  Hyperammonemia [MESH:D022124] (322)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Leukocytosis [MESH:D007964] (978)  Muscle Weakness [MESH:D018908] (478)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Sclerosis [MESH:D012598] (224)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Long QT Syndrome [MESH:D008133] (691)  Ventricular Fibrillation [MESH:D014693] (624)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Heart Block [MESH:D006327] (571)   Sick Sinus Syndrome [MESH:D012804] (293)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Chromosome Aberrations [MESH:D002869] (2352)   Translocation, Genetic [MESH:D014178] (557)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Disease Attributes [MESH:D020969] (3654)   Critical Illness [MESH:D016638] (296)  Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Growth Disorders [MESH:D006130] (2438)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Hemorrhage [MESH:D006470] (4451)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Hematuria [MESH:D006417] (477)  Shock, Hemorrhagic [MESH:D012771] (2042)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Hyperbilirubinemia [MESH:D006932] (1860)   Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  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)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Necrosis [MESH:D009336] (4019)   Osteonecrosis [MESH:D010020] (537)   Femur Head Necrosis [MESH:D005271] (266)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Pain, Postoperative [MESH:D010149] (529)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Cardiogenic [MESH:D012770] (269)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Asthenia [MESH:D001247] (376)  Cardiac Output, High [MESH:D016534] (123)  Edema [MESH:D004487] (3726)  Fatigue [MESH:D005221] (437)  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)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Eye Manifestations [MESH:D005132] (213)   Eye Pain [MESH:D058447] (207)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Neurologic Manifestations [MESH:D009461] (8702)   Reflex, Abnormal [MESH:D012021] (485)  Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Ataxia [MESH:D001259] (984)   Cerebellar Ataxia [MESH:D002524] (289)  Gait Ataxia [MESH:D020234] (26)  Gait Disorders, Neurologic [MESH:D020233] (491)   Gait Ataxia [MESH:D020234] (26)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Consciousness Disorders [MESH:D003244] (677)  Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Facial Paralysis [MESH:D005158] (238)  Quadriplegia [MESH:D011782] (115)  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)   Charcot-Marie-Tooth Disease, Demyelinating, Type 1e [MESH:C566136] (76)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Charcot-Marie-Tooth disease, Type 2J [MESH:C535417] (22)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Taste Disorders [MESH:D013651] (461)   Dysgeusia [MESH:D004408] (24)  Pain [MESH:D010146] (4511)   Arthralgia [MESH:D018771] (191)  Eye Pain [MESH:D058447] (207)  Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Pain, Postoperative [MESH:D010149] (529)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Constipation [MESH:D003248] (506)  Diarrhea [MESH:D003967] (858)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Dyspnea [MESH:D004417] (248)  Respiratory Sounds [MESH:D012135] (713)  Skin Manifestations [MESH:D012877] (1250)   Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Urological Manifestations [MESH:D020924] (3532)   Hypercalciuria [MESH:D053565] (330)  Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Virilism [MESH:D014770] (327)   Hirsutism [MESH:D006628] (323) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Drug Hypersensitivity [MESH:D004342] (4001)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2697)   Hand-Foot Syndrome [MESH:D060831] (4)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Lead Poisoning [MESH:D007855] (515)  Manganese Poisoning [MESH:D020149] (2214)  Neurotoxicity Syndromes [MESH:D020258] (3323)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950)  Morphine Dependence [MESH:D009021] (855) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Alicyclic [MESH:D006840] (3199)   Cycloparaffins [MESH:D003516] (3197)   Cyclodecanes [MESH:D043822] (268)   Taxoids [MESH:D043823] (265)  Terpenes [MESH:D013729] (10347)   Diterpenes [MESH:D004224] (2867)   Taxoids [MESH:D043823] (265) D27. Chemical Actions and Uses  D27. Chemical Actions and Uses  Pharmacologic Actions [MESH:D020228] (2566)   Molecular Mechanisms of Pharmacological Action [MESH:D045504] (1155)   Mitosis Modulators [MESH:D050258] (20)   Antimitotic Agents [MESH:D050256] (13)   Tubulin Modulators [MESH:D050257] (12)  Therapeutic Uses [MESH:D045506] (1611)   Antineoplastic Agents [MESH:D000970] (319) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Diagnostic Imaging [MESH:D003952] (623)   Ultrasonography [MESH:D014463] (482)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Diagnostic Techniques, Cardiovascular [MESH:D003935] (521)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Physical Examination [MESH:D010808] (1041)   Body Constitution [MESH:D001824] (450)   Body Weights and Measures [MESH:D001837] (448)   Body Size [MESH:D049628] (439)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407) 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)  Physiological Phenomena [MESH:D010829] (788)   Body Constitution [MESH:D001824] (453)   Body Weights and Measures [MESH:D001837] (444)   Body Size [MESH:D049628] (438)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Circulatory and Respiratory Physiological Phenomena [MESH:D002943] (614)   Cardiovascular Physiological Phenomena [MESH:D002320] (525)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)