Item 28 of 41 (back to results) previous next   Enalapril D004656               MeSH Unique Identifier: D004656 Scope Notes: One of the ANGIOTENSIN-CONVERTING ENZYME INHIBITORS that is used to treat hypertension. Chemical – Gene Interaction Note 1: ABCC4 protein results in increased transport of Enalapril Note 2: ACE gene polymorphism affects the susceptibility to [Enalapril co-treated with Sodium Chloride] Click here for more information

Current search: C07. Stomatognathic Diseases: Stomatognathic Diseases [MESH:D009057] > Tooth Diseases [MESH:D014076] > Failure of Tooth Eruption, Primary [MESH:C565114] × 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 C [HGNC:ABCC] (458)   ATP-binding cassette, sub-family C (CFTR/MRP), member 4 [HGNC:ABCC4] (88)  CD molecules [HGNC:CD] (1459)   angiotensin I converting enzyme [HGNC:ACE] (39)  coagulation factor III (thromboplastin, tissue factor) [HGNC:F3] (92)  toll-like receptor 4 [HGNC:TLR4] (62)  Interferons and interferon receptors [HGNC:IFN] (684)   interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 01, alpha [HGNC:IL1A] (157)  interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)  RING-type zinc fingers [HGNC:RNF] (151)   TNF receptor-associated factor 6, E3 ubiquitin protein ligase [HGNC:TRAF6] (24)  Solute carriers [HGNC:SLC] (716)   solute carrier family 15 (oligopeptide transporter), member 2 [HGNC:SLC15A2] (14)  solute carrier organic anion transporter family, member 1B1 [HGNC:SLCO1B1] (60)  Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898)   tumor necrosis factor [HGNC:TNF] (795) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   abundance (136)  cotreatment (1499)  response to substance (623)  Decreases (5154)   activity (2549)  expression (2187)  reaction (3393)  Increases (5571)   abundance (630)  activity (2865)  expression (3238)  response to substance (641)  transport (399)  uptake (378) A. Anatomy  A. Anatomy  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   Nephrons [MESH:D009399] (518)   Kidney Tubules [MESH:D007684] (510)   Kidney Tubules, Proximal [MESH:D007687] (504)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Cardiovascular System [MESH:D002319] (1086)   Blood Vessels [MESH:D001808] (278)   Arteries [MESH:D001158] (173)   Retinal Artery [MESH:D012161] (78)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Retinal Vessels [MESH:D012171] (112)   Retinal Artery [MESH:D012161] (78)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Heart [MESH:D006321] (904)   Heart Atria [MESH:D006325] (65)   Atrial Standstill [MESH:C563984] (32)  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)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Uvea [MESH:D014602] (270)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221) 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)  Neisseriaceae Infections [MESH:D016870] (273)   Meningococcal Infections [MESH:D008589] (242)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Tuberculosis [MESH:D014376] (992)   Tuberculosis, Pulmonary [MESH:D014397] (678)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Urinary Tract Infections [MESH:D014552] (984)  Intraabdominal Infections [MESH:D059413] (958)   Peritonitis [MESH:D010538] (800)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Pneumonia, Viral [MESH:D011024] (125)  Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Herpesviridae Infections [MESH:D006566] (1944)   Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  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)   Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Nidovirales Infections [MESH:D030341] (136)   Coronaviridae Infections [MESH:D003333] (133)   Coronavirus Infections [MESH:D018352] (131)   Severe Acute Respiratory Syndrome [MESH:D045169] (127)  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) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Helminthiasis [MESH:D006373] (1644)   Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   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, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  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)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Leiomyosarcoma [MESH:D007890] (977)  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)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Keratoacanthoma familial [MESH:C536150] (78)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma in Situ [MESH:D002278] (2111)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Lobular [MESH:D018275] (305)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Lobular [MESH:D018275] (305)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioma, capillary infantile [MESH:C535860] (190)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  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)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   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)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   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)  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)   Hemangioma, capillary infantile [MESH:C535860] (190)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  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)   Cartilage Diseases [MESH:D002357] (438)  Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromicric dysplasia [MESH:C535662] (520)  Dwarfism [MESH:D004392] (778)   Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Osteochondrodysplasias [MESH:D010009] (2440)   Jansen type metaphyseal chondrodysplasia [MESH:C537564] (40)  Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Eiken Skeletal Dysplasia [MESH:C564010] (40)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Enchondromatosis [MESH:D004687] (170)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Bone Diseases, Endocrine [MESH:D001849] (747)   Acromegaly [MESH:D000172] (466)  Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Rickets [MESH:D012279] (341)  Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)  Hyperostosis [MESH:D015576] (493)   Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Exostoses [MESH:D005096] (160)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Eiken Skeletal Dysplasia [MESH:C564010] (40)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Eiken Skeletal Dysplasia [MESH:C564010] (40)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Joint Diseases [MESH:D007592] (4657)   Arthralgia [MESH:D018771] (191)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Psoriatic [MESH:D015535] (1859)  Osteoarthritis [MESH:D010003] (1743)  Arthritis, Rheumatoid [MESH:D001172] (3603)   Sjogren's Syndrome [MESH:D012859] (17)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Myopathy, Myosin Storage [MESH:C564253] (77)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Brachydactyly [MESH:D059327] (220)   Brachydactyly with hypertension [MESH:C537095] (4)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Eiken Skeletal Dysplasia [MESH:C564010] (40)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Eiken Skeletal Dysplasia [MESH:C564010] (40)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Osteoarthritis [MESH:D010003] (1743)  Arthritis, Rheumatoid [MESH:D001172] (3603)   Sjogren's Syndrome [MESH:D012859] (17) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   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)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Stenosis [MESH:D004940] (490)  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)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Intestinal Perforation [MESH:D007416] (471)  Colonic Diseases [MESH:D003108] (5564)   Megacolon [MESH:D008531] (386)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   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 B, Chronic [MESH:D019694] (277)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  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)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Peritoneal Diseases [MESH:D010532] (1119)   Peritoneal Fibrosis [MESH:D056627] (488)  Peritonitis [MESH:D010538] (800) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   PCI 5002 [MESH:C568608] (527)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Oral Ulcer [MESH:D019226] (488)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   PCI 5002 [MESH:C568608] (433)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   PCI 5002 [MESH:C568608] (433)  Cleft Palate [MESH:D002972] (1330)   Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Salivary Gland Diseases [MESH:D012466] (1213)   Sialorrhea [MESH:D012798] (252)  Xerostomia [MESH:D014987] (98)   Sjogren's Syndrome [MESH:D012859] (17)   Pancreatitis, Sclerosing Cholangitis, and Sicca Complex [MESH:C564906] (13)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Tongue Diseases [MESH:D014060] (1544)   Macroglossia [MESH:D008260] (7)   Congenital macroglossia [MESH:C531735] (6)  Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  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)   Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 12 [MESH:C567548] (434)  Cleft Palate [MESH:D002972] (1330)   Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Tooth Diseases [MESH:D014076] (742)   Failure of Tooth Eruption, Primary [MESH:C565114] (41) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Respiratory System Abnormalities [MESH:D015619] (243)  Bronchial Diseases [MESH:D001982] (4382)   Bronchial Hyperreactivity [MESH:D016535] (1357)  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)   Cystic Fibrosis [MESH:D003550] (760)  Hypertension, Pulmonary [MESH:D006976] (2000)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Alveolitis, Extrinsic Allergic [MESH:D000542] (496)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Pneumonia, Viral [MESH:D011024] (125)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Cough [MESH:D003371] (179)  Dyspnea [MESH:D004417] (248)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Obstructive [MESH:D020181] (126)  Respiratory Insufficiency [MESH:D012131] (841)   Airway Obstruction [MESH:D000402] (191)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  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)  Severe Acute Respiratory Syndrome [MESH:D045169] (127)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Pneumonia, Viral [MESH:D011024] (125)  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)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Retrocochlear Diseases [MESH:D012181] (241)   Auditory Diseases, Central [MESH:D001304] (210)   Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  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)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Vasculitis, Central Nervous System [MESH:D020293] (28)   Giant Cell Arteritis [MESH:D013700] (10)  Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Multiple System Atrophy [MESH:D019578] (102)   Shy-Drager Syndrome [MESH:D012791] (99)  Orthostatic Intolerance [MESH:D054971] (720)   Hypotension, Orthostatic [MESH:D007024] (679)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Familial porencephaly [MESH:C536850] (77)  Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Auditory Diseases, Central [MESH:D001304] (210)   Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Multiple System Atrophy [MESH:D019578] (158)   Shy-Drager Syndrome [MESH:D012791] (99)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebrovascular Disorders [MESH:D002561] (5542)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Vertebrobasilar Insufficiency [MESH:D014715] (9)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Moyamoya Disease [MESH:D009072] (10)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Moyamoya Disease [MESH:D009072] (10)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Vasculitis, Central Nervous System [MESH:D020293] (28)   Giant Cell Arteritis [MESH:D013700] (10)  Dementia [MESH:D003704] (4498)   Lewy Body Disease [MESH:D020961] (1143)  Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  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)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)   Migraine without Aura [MESH:D020326] (408)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Hyperpituitarism [MESH:D006964] (1250)   Acromegaly [MESH:D000172] (466)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Hypopituitarism [MESH:D007018] (732)   Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Inappropriate ADH Syndrome [MESH:D007177] (178)   Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Leukoencephalopathies [MESH:D056784] (1916)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  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)  Prion Diseases [MESH:D017096] (488)   Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Dystonic Disorders [MESH:D020821] (729)   Dystonia 12 [MESH:C538001] (36)  Multiple System Atrophy [MESH:D019578] (158)   Shy-Drager Syndrome [MESH:D012791] (99)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Vestibulocochlear Nerve Diseases [MESH:D000160] (111)   Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Nervous System Malformations [MESH:D009421] (3354)   Malformations of Cortical Development [MESH:D054220] (1406)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Shy-Drager Syndrome [MESH:D012791] (99)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hepatolenticular Degeneration [MESH:D006527] (473)  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)  Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37)  Multiple System Atrophy [MESH:D019578] (158)   Shy-Drager Syndrome [MESH:D012791] (99)  Prion Diseases [MESH:D017096] (475)   Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37)  Neurologic Manifestations [MESH:D009461] (8964)   Gait Disorders, Neurologic [MESH:D020233] (491)  Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Consciousness Disorders [MESH:D003244] (680)   Unconsciousness [MESH:D014474] (660)   Syncope [MESH:D013575] (128)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypertonia [MESH:D009122] (775)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Hemiplegia [MESH:D006429] (184)   Alternating hemiplegia of childhood [MESH:C536589] (70)  Familial porencephaly [MESH:C536850] (77)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Pupil Disorders [MESH:D011681] (194)   Pierson syndrome [MESH:C537185] (33)  Sensation Disorders [MESH:D012678] (5011)   Dizziness [MESH:D004244] (289)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  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)  Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37)  Muscular Diseases [MESH:D009135] (3538)   Myopathy, Myosin Storage [MESH:C564253] (77)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Polyneuropathies [MESH:D011115] (1134)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)  Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Obstructive [MESH:D020181] (126)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Eye Abnormalities [MESH:D005124] (1233)   Pierson syndrome [MESH:C537185] (33)  Coloboma [MESH:D003103] (315)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Eye Hemorrhage [MESH:D005130] (94)   Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)   Sjogren's Syndrome [MESH:D012859] (17)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma, Open-Angle [MESH:D005902] (1281)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Pupil Disorders [MESH:D011681] (230)   Pierson syndrome [MESH:C537185] (33)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinopathy of Prematurity [MESH:D012178] (353)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Macular Degeneration, Age-Related, 10 [MESH:C566935] (162)  Macular Edema [MESH:D008269] (557)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Testicular Diseases [MESH:D013733] (451)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Penile Diseases [MESH:D010409] (1805)   Penile Induration [MESH:D010411] (495)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Urogenital Abnormalities [MESH:D014564] (2065)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Gonadal Dysgenesis [MESH:D006059] (492)   Turner Syndrome [MESH:D014424] (131)  Sex Chromosome Disorders of Sex Development [MESH:D058533] (137)   Turner Syndrome [MESH:D014424] (131)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Lipoprotein Glomerulopathy [MESH:C567089] (165)  Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Cortex Necrosis [MESH:D007673] (25)  Nephrosclerosis [MESH:D009400] (18)  Renal Artery Obstruction [MESH:D012078] (15)  Diabetes Insipidus [MESH:D003919] (354)   Diabetes Insipidus, Nephrogenic [MESH:D018500] (90)  Diabetes Insipidus, Neurogenic [MESH:D020790] (100)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrosis [MESH:D009401] (2228)   Nephrosis, Lipoid [MESH:D009402] (74)  Nephrotic Syndrome [MESH:D009404] (1536)   Pierson syndrome [MESH:C537185] (33)  Mesangial sclerosis, diffuse [MESH:C537346] (33)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Renal hypouricemia [MESH:C537757] (71)  Bartter Syndrome [MESH:D001477] (241)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Glycosuria [MESH:D006029] (100)  Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urinary Incontinence [MESH:D014549] (81)   Urinary Incontinence, Stress [MESH:D014550] (8)  Urolithiasis [MESH:D052878] (585)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Uterine Diseases [MESH:D014591] (2479)   Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Urogenital Abnormalities [MESH:D014564] (2043)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Gonadal Dysgenesis [MESH:D006059] (492)   Turner Syndrome [MESH:D014424] (131)  Sex Chromosome Disorders of Sex Development [MESH:D058533] (137)   Turner Syndrome [MESH:D014424] (131)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Lipoprotein Glomerulopathy [MESH:C567089] (165)  Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Cortex Necrosis [MESH:D007673] (25)  Nephrosclerosis [MESH:D009400] (18)  Renal Artery Obstruction [MESH:D012078] (15)  Diabetes Insipidus [MESH:D003919] (354)   Diabetes Insipidus, Nephrogenic [MESH:D018500] (90)  Diabetes Insipidus, Neurogenic [MESH:D020790] (100)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrosis [MESH:D009401] (2228)   Nephrosis, Lipoid [MESH:D009402] (74)  Nephrotic Syndrome [MESH:D009404] (1536)   Pierson syndrome [MESH:C537185] (33)  Mesangial sclerosis, diffuse [MESH:C537346] (33)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Renal hypouricemia [MESH:C537757] (71)  Bartter Syndrome [MESH:D001477] (241)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Glycosuria [MESH:D006029] (100)  Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urinary Incontinence [MESH:D014549] (81)   Urinary Incontinence, Stress [MESH:D014550] (8)  Urolithiasis [MESH:D052878] (585)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Oligohydramnios [MESH:D016104] (9)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Fetal Diseases [MESH:D005315] (1206)   Chorioamnionitis [MESH:D002821] (313)  Fetal Growth Retardation [MESH:D005317] (986)  Erythroblastosis, Fetal [MESH:D004899] (24)   Hydrops Fetalis [MESH:D015160] (23)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Abruptio Placentae [MESH:D000037] (430)  Obstetric Labor, Premature [MESH:D007752] (1316)  Fetal Membranes, Premature Rupture [MESH:D005322] (356)   Chorioamnionitis [MESH:D002821] (313)  Placenta Diseases [MESH:D010922] (1781)   Abruptio Placentae [MESH:D000037] (430)  Chorioamnionitis [MESH:D002821] (313)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) 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)   Ductus Arteriosus, Patent [MESH:D004374] (325)  Turner Syndrome [MESH:D014424] (131)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  Heart Septal Defects, Atrial [MESH:D006344] (209)   Atrial septal defect 2 [MESH:C538263] (69)  Vascular Malformations [MESH:D054079] (1098)   Arteriovenous Malformations [MESH:D001165] (1058)   Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62)  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)   Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial fibrillation, familial 1 [MESH:C538261] (32)  Atrial Fibrillation, Familial, 6 [MESH:C567400] (196)  Cardiac Complexes, Premature [MESH:D005117] (429)   Ventricular Premature Complexes [MESH:D018879] (418)  Heart Block [MESH:D006327] (571)   Atrial Standstill [MESH:C563984] (32)  Sick Sinus Syndrome [MESH:D012804] (293)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Hypertrophy, Right Ventricular [MESH:D017380] (136)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1s [MESH:C563538] (77)  Cardiomyopathy, Dilated, 1EE [MESH:C567683] (61)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Atrial Standstill [MESH:C563984] (32)  Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Endomyocardial Fibrosis [MESH:D004719] (521)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1s [MESH:C563538] (77)  Cardiomyopathy, Dilated, 1EE [MESH:C567683] (61)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 14 [MESH:C567684] (61)  Heart Defects, Congenital [MESH:D006330] (2443)   Ductus Arteriosus, Patent [MESH:D004374] (325)  Turner Syndrome [MESH:D014424] (131)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  Heart Septal Defects, Atrial [MESH:D006344] (209)   Atrial septal defect 2 [MESH:C538263] (69)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Mitral Valve Insufficiency [MESH:D008944] (35)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Vasospasm [MESH:D003329] (533)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  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)  Vascular Diseases [MESH:D014652] (8691)   Hyperemia [MESH:D006940] (2372)  Retinal Vein Occlusion [MESH:D012170] (607)  Superior Vena Cava Syndrome [MESH:D013479] (64)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Angioedema [MESH:D000799] (837)   Acquired angioedema [MESH:C538173] (157)  Angioedemas, Hereditary [MESH:D054179] (224)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Carotid Stenosis [MESH:D016893] (174)  Moyamoya Disease [MESH:D009072] (10)  Renal Artery Obstruction [MESH:D012078] (15)  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)   Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Arteritis [MESH:D001167] (1084)   Giant Cell Arteritis [MESH:D013700] (10)  Polyarteritis Nodosa [MESH:D010488] (25)  Cerebrovascular Disorders [MESH:D002561] (5541)   Vertebrobasilar Insufficiency [MESH:D014715] (9)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Vertebrobasilar Insufficiency [MESH:D014715] (9)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Moyamoya Disease [MESH:D009072] (10)  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)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Moyamoya Disease [MESH:D009072] (10)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Vasculitis, Central Nervous System [MESH:D020293] (28)   Giant Cell Arteritis [MESH:D013700] (10)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Hypertension [MESH:D006973] (5655)   Brachydactyly with hypertension [MESH:C537095] (4)  Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy [MESH:C565359] (84)  Hypertension, Malignant [MESH:D006974] (621)  Hypertension, Pregnancy-Induced [MESH:D046110] (397)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  Shy-Drager Syndrome [MESH:D012791] (99)  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 Vasospasm [MESH:D003329] (533)  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)   Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Raynaud Disease [MESH:D011928] (490)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Telangiectasis [MESH:D013684] (255)   Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784)  Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Vasculitis, Leukocytoclastic, Cutaneous [MESH:D018366] (121)  Arteritis [MESH:D001167] (1084)   Giant Cell Arteritis [MESH:D013700] (10)  Polyarteritis Nodosa [MESH:D010488] (25)  Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76)  Systemic Vasculitis [MESH:D056647] (71)   Polyarteritis Nodosa [MESH:D010488] (25)  Vasculitis, Central Nervous System [MESH:D020293] (28)   Giant Cell Arteritis [MESH:D013700] (10) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Pancytopenia [MESH:D010198] (332)  Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Hemolytic [MESH:D000743] (3083)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Blood Coagulation Disorders [MESH:D001778] (1828)   Flaujeac factor deficiency [MESH:C537060] (117)  Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Hydrops Fetalis [MESH:D015160] (23)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)  Myeloproliferative Disorders [MESH:D009196] (1492)   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)  alpha-Thalassemia [MESH:D017085] (192)   Hydrops Fetalis [MESH:D015160] (23)  Hemorrhagic Disorders [MESH:D006474] (3359)   Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328)  Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Leukocyte Disorders [MESH:D007960] (2662)   Eosinophilia [MESH:D004802] (537)  Leukocytosis [MESH:D007964] (988)  Leukostasis [MESH:D018921] (769)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)  Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Polycythemia [MESH:D011086] (412)   Polycythemia, primary familial and congenital [MESH:C536842] (45)  Thrombophilia [MESH:D019851] (592)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Lymphatic Diseases [MESH:D008206] (5167)   Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Drug-Induced [MESH:D000014] (1024)  Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Pierson syndrome [MESH:C537185] (33)  Down Syndrome [MESH:D004314] (1287)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Ductus Arteriosus, Patent [MESH:D004374] (325)  Turner Syndrome [MESH:D014424] (131)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Ventricular [MESH:D006345] (160)  Heart Septal Defects, Atrial [MESH:D006344] (209)   Atrial septal defect 2 [MESH:C538263] (69)  Vascular Malformations [MESH:D054079] (1108)   Arteriovenous Malformations [MESH:D001165] (1058)   Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1018)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)   Osler-rendu-weber syndrome 2 [MESH:C537139] (34)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Sex Chromosome Disorders [MESH:D025064] (479)   Sex Chromosome Disorders of Sex Development [MESH:D058533] (136)   Turner Syndrome [MESH:D014424] (131)  Eye Abnormalities [MESH:D005124] (1233)   Pierson syndrome [MESH:C537185] (33)  Coloboma [MESH:D003103] (315)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Brachydactyly [MESH:D059327] (220)   Brachydactyly with hypertension [MESH:C537095] (4)  Foot Deformities, Congenital [MESH:D005532] (538)   Eiken Skeletal Dysplasia [MESH:C564010] (40)  Hand Deformities, Congenital [MESH:D006228] (587)   Eiken Skeletal Dysplasia [MESH:C564010] (40)  Nervous System Malformations [MESH:D009421] (3354)   Malformations of Cortical Development [MESH:D054220] (1406)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Skin Abnormalities [MESH:D012868] (1723)   Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  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)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Gonadal Dysgenesis [MESH:D006059] (492)   Turner Syndrome [MESH:D014424] (131)  Sex Chromosome Disorders of Sex Development [MESH:D058533] (137)   Turner Syndrome [MESH:D014424] (131)  Fetal Diseases [MESH:D005315] (1205)   Chorioamnionitis [MESH:D002821] (313)  Fetal Growth Retardation [MESH:D005317] (986)  Erythroblastosis, Fetal [MESH:D004899] (24)   Hydrops Fetalis [MESH:D015160] (23)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Atrial Standstill [MESH:C563984] (32)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Angioedemas, Hereditary [MESH:D054179] (172)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Cystic Fibrosis [MESH:D003550] (760)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 14 [MESH:C567684] (61)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Sex Chromosome Disorders [MESH:D025064] (479)   Sex Chromosome Disorders of Sex Development [MESH:D058533] (136)   Turner Syndrome [MESH:D014424] (131)  Dwarfism [MESH:D004392] (783)   Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  alpha-Thalassemia [MESH:D017085] (192)   Hydrops Fetalis [MESH:D015160] (23)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hepatolenticular Degeneration [MESH:D006527] (473)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease Type V [MESH:D006012] (165)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Adrenoleukodystrophy [MESH:D000326] (1348)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Renal hypouricemia [MESH:C537757] (71)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Muscular Dystrophies [MESH:D009136] (1597)   Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Chondrodysplasia, blomstrand type [MESH:C537914] (40)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Skin Diseases, Genetic [MESH:D012873] (3456)   Darier Disease [MESH:D007644] (125)  Dermatitis, Atopic [MESH:D003876] (2052)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Cystic Fibrosis [MESH:D003550] (760)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Retinopathy of Prematurity [MESH:D012178] (353) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Cartilage Diseases [MESH:D002357] (438)  Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Penile Induration [MESH:D010411] (495)  Scleroderma, Localized [MESH:D012594] (1597)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)   Sjogren's Syndrome [MESH:D012859] (17)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Exanthema [MESH:D005076] (301)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Pruritus [MESH:D011537] (647)  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)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Keratoacanthoma [MESH:D007636] (83)   Keratoacanthoma familial [MESH:C536150] (78)  Keratosis [MESH:D007642] (1941)   Darier Disease [MESH:D007644] (125)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Skin Abnormalities [MESH:D012868] (1709)   Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  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)   Darier Disease [MESH:D007644] (125)  Dermatitis, Atopic [MESH:D003876] (2052)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Skin Diseases, Infectious [MESH:D012874] (2684)   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)   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)   Behcet Syndrome [MESH:D001528] (1784)  Giant Cell Arteritis [MESH:D013700] (10)  Polyarteritis Nodosa [MESH:D010488] (25)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Acquired angioedema [MESH:C538173] (157)  Angioedemas, Hereditary [MESH:D054179] (224)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Z. Exceptions (817)   Not Fully Specified [NFS] (817)  Metabolic Diseases [MESH:D008659] (9025)   Acid-Base Imbalance [MESH:D000137] (854)   Alkalosis [MESH:D000471] (384)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Rickets [MESH:D012279] (341)  Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Fanconi Anemia [MESH:D005199] (1604)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Glycosuria [MESH:D006029] (100)  Hypoglycemia [MESH:D007003] (2420)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Iron Metabolism Disorders [MESH:D019189] (2139)   Anemia, Iron-Deficiency [MESH:D018798] (547)  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)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hypertriglyceridemia [MESH:D015228] (808)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease Type V [MESH:D006012] (165)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Adrenoleukodystrophy [MESH:D000326] (1348)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Renal hypouricemia [MESH:C537757] (71)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Mitochondrial Diseases [MESH:D028361] (2561)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Dehydration [MESH:D003681] (121)  Hypercalcemia [MESH:D006934] (1999)  Hyperkalemia [MESH:D006947] (485)  Hypokalemia [MESH:D007008] (1041)  Hyponatremia [MESH:D007010] (789)  Inappropriate ADH Syndrome [MESH:D007177] (178)   Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Vitamin D Deficiency [MESH:D014808] (360)   Rickets [MESH:D012279] (341)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Obesity, Morbid [MESH:D009767] (515)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Hyperaldosteronism [MESH:D006929] (419)   Bartter Syndrome [MESH:D001477] (241)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Dwarfism [MESH:D004392] (698)   Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Gonadal Disorders [MESH:D006058] (5088)   Hypogonadism [MESH:D007006] (1123)  Puberty, Precocious [MESH:D011629] (1147)  Testicular Diseases [MESH:D013733] (777)  Disorders of Sex Development [MESH:D012734] (1637)   Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Gonadal Dysgenesis [MESH:D006059] (492)   Turner Syndrome [MESH:D014424] (131)  Sex Chromosome Disorders of Sex Development [MESH:D058533] (137)   Turner Syndrome [MESH:D014424] (131)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Pituitary Diseases [MESH:D010900] (1829)   Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)  Diabetes Insipidus [MESH:D003919] (302)   Diabetes Insipidus, Neurogenic [MESH:D020790] (100)  Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Hypopituitarism [MESH:D007018] (732)   Dwarfism, Pituitary [MESH:D004393] (235)   Kowarski syndrome [MESH:C537505] (129)  Isolated Growth Hormone Deficiency, Type II [MESH:C562704] (129)  Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Inappropriate ADH Syndrome [MESH:D007177] (178)   Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Arthritis, Rheumatoid [MESH:D001172] (3601)   Sjogren's Syndrome [MESH:D012859] (17)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Vasculitis, Central Nervous System [MESH:D020293] (27)   Giant Cell Arteritis [MESH:D013700] (10)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Hydrops Fetalis [MESH:D015160] (23)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2695)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Anaphylaxis [MESH:D000707] (299)  Asthma, Aspirin-Induced [MESH:D055963] (1055)  Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (3914)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Acquired angioedema [MESH:C538173] (157)  Angioedemas, Hereditary [MESH:D054179] (224)  Immune Complex Diseases [MESH:D007105] (782)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Vasculitis, Leukocytoclastic, Cutaneous [MESH:D018366] (121)  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)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative [MESH:C565533] (111)  Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Plaque, Atherosclerotic [MESH:D058226] (696)  Ventricular Remodeling [MESH:D020257] (686)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Hypertrophy [MESH:D006984] (4476)   Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Hypertrophy, Right Ventricular [MESH:D017380] (136)  Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Ascites [MESH:D001201] (139)  Azotemia [MESH:D053099] (326)  Dehydration [MESH:D003681] (121)  Emphysema [MESH:D004646] (1096)  Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506)  Hyperplasia [MESH:D006965] (2463)  Hypovolemia [MESH:D020896] (12)  Ischemia [MESH:D007511] (3049)  Leukocytosis [MESH:D007964] (978)  Necrosis [MESH:D009336] (4019)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial fibrillation, familial 1 [MESH:C538261] (32)  Atrial Fibrillation, Familial, 6 [MESH:C567400] (196)  Cardiac Complexes, Premature [MESH:D005117] (429)   Ventricular Premature Complexes [MESH:D018879] (418)  Heart Block [MESH:D006327] (571)   Atrial Standstill [MESH:C563984] (32)  Sick Sinus Syndrome [MESH:D012804] (293)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Fibrosis [MESH:D005355] (3133)   Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Granuloma [MESH:D006099] (587)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Growth Disorders [MESH:D006130] (2438)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Eye Hemorrhage [MESH:D005130] (94)   Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Hyperbilirubinemia [MESH:D006932] (1860)   Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Inflammation [MESH:D007249] (5241)   Acute-Phase Reaction [MESH:D000210] (40)  Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Menstruation Disturbances [MESH:D008599] (926)   Dysmenorrhea [MESH:D004412] (189)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Sclerosis [MESH:D012598] (224)   Mesangial sclerosis, diffuse [MESH:C537346] (33)  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)  Cyanosis [MESH:D003490] (288)  Fatigue [MESH:D005221] (437)  Flushing [MESH:D005483] (506)  Reticulocytosis [MESH:D045262] (514)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Birth Weight [MESH:D001724] (377)  Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)   Obesity, Morbid [MESH:D009767] (515)  Edema [MESH:D004487] (3726)   Hydrops Fetalis [MESH:D015160] (23)  Neurologic Manifestations [MESH:D009461] (8702)   Gait Disorders, Neurologic [MESH:D020233] (491)  Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Consciousness Disorders [MESH:D003244] (677)   Unconsciousness [MESH:D014474] (657)   Syncope [MESH:D013575] (128)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypertonia [MESH:D009122] (775)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Hemiplegia [MESH:D006429] (184)   Alternating hemiplegia of childhood [MESH:C536589] (70)  Familial porencephaly [MESH:C536850] (77)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Pupil Disorders [MESH:D011681] (194)   Pierson syndrome [MESH:C537185] (33)  Sensation Disorders [MESH:D012678] (5009)   Dizziness [MESH:D004244] (289)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  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)  Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Abdominal Pain [MESH:D015746] (248)   Abdomen, Acute [MESH:D000006] (5)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Pelvic Pain [MESH:D017699] (198)   Dysmenorrhea [MESH:D004412] (189)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Diarrhea [MESH:D003967] (858)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Abdominal Pain [MESH:D015746] (248)   Abdomen, Acute [MESH:D000006] (5)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Cough [MESH:D003371] (179)  Dyspnea [MESH:D004417] (248)  Hypercapnia [MESH:D006935] (264)  Skin Manifestations [MESH:D012877] (1250)   Pruritus [MESH:D011537] (648)  Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Urological Manifestations [MESH:D020924] (3532)   Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Lower Urinary Tract Symptoms [MESH:D059411] (612)   Urinary Bladder, Overactive [MESH:D053201] (530)  Urinary Incontinence [MESH:D014549] (81)   Urinary Incontinence, Stress [MESH:D014550] (8)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Manganese Poisoning [MESH:D020149] (2214)  Mercury Poisoning [MESH:D008630] (193)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Drug Overdose [MESH:D062787] (513)  Marijuana Abuse [MESH:D002189] (1132)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D12. Amino Acids, Peptides, and Proteins  D12. Amino Acids, Peptides, and Proteins  Peptides [MESH:D010455] (20561)   Oligopeptides [MESH:D009842] (4990)   Dipeptides [MESH:D004151] (1035)   Enalapril [MESH:D004656] (9) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Diagnostic Imaging [MESH:D003952] (623)   Ultrasonography [MESH:D014463] (482)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Diagnostic Techniques, Cardiovascular [MESH:D003935] (521)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Mental Disorders [MESH:D001523] (2063)   Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Dementia [MESH:D003704] (471)   Alzheimer Disease [MESH:D000544] (242)   Alzheimer disease type 2 [MESH:C536595] (165) G. Phenomena and Processes  G. Phenomena and Processes  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)