Item 6 of 82 (back to results) previous next   nitrosobenzylmethylamine C014707               MeSH Unique Identifier: C014707 Chemical – Gene Interaction Note 1: CYP2E1 protein affects the metabolism of nitrosobenzylmethylamine Click here for more information

Current search: C26. Wounds and Injuries: Wounds and Injuries [MESH:D014947] > Thoracic Injuries [MESH:D013898] > Heart Injuries [MESH:D006335] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 02, subfamily E, polypeptide 01 [HGNC:CYP2E1] (225) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   metabolic processing (485) 4. Semantic Terms  4. Semantic Terms  Entity [STY:T071] (48056)   Physical Object [STY:T072] (47583)   Substance [STY:T167] (46174)   Chemical [STY:T103] (46110)   Chemical Viewed Functionally [STY:T120] (28747)   Pharmacologic Substance [STY:T121] (11019)  Chemical Viewed Structurally [STY:T104] (44741)   Organic Chemical [STY:T109] (44144) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Breast [MESH:D001940] (56)   Limb-mammary syndrome [MESH:C535903] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Extremities [MESH:D005121] (484)   Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Meier-Gorlin syndrome [MESH:C538012] (133)  Face [MESH:D005145] (387)   Eye [MESH:D005123] (148)   Eyelids [MESH:D005143] (143)   Hay-Wells syndrome [MESH:C535847] (46)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Leg Bones [MESH:D007867] (228)   Patella [MESH:D010329] (168)   Meier-Gorlin syndrome [MESH:C538012] (133)  Endocrine System [MESH:D004703] (206)   Endocrine Glands [MESH:D004702] (193)   Thyroid Gland [MESH:D013961] (53)   Thyroid Dyshormonogenesis 3 [MESH:C562769] (46)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Atria [MESH:D006325] (65)   Atrial myxoma, familial [MESH:C538262] (34)  Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Meier-Gorlin syndrome [MESH:C538012] (133)  Eye [MESH:D005123] (858)   Eyelids [MESH:D005143] (146)   Hay-Wells syndrome [MESH:C535847] (46)  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Cell Surface Extensions [MESH:D022081] (43)   Microvilli [MESH:D008871] (29)   Microvillus inclusion disease [MESH:C537470] (28) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Tuberculosis [MESH:D014376] (992)   Tuberculosis, Pulmonary [MESH:D014397] (678)  Skin Diseases, Bacterial [MESH:D017192] (157)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Infection [MESH:D007239] (4109)   Urinary Tract Infections [MESH:D014552] (984)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Skin Diseases, Infectious [MESH:D012874] (415)   Skin Diseases, Bacterial [MESH:D017192] (156)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Suppuration [MESH:D013492] (219)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Poliomyelitis [MESH:D011051] (54)  Myelitis [MESH:D009187] (71)   Poliomyelitis [MESH:D011051] (56)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)  Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Picornaviridae Infections [MESH:D010850] (1672)   Enterovirus Infections [MESH:D004769] (241)   Poliomyelitis [MESH:D011051] (56)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   HIV Wasting Syndrome [MESH:D019247] (1956)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   Trematode Infections [MESH:D014201] (1182)   Opisthorchiasis [MESH:D009889] (160)  Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Protozoan Infections [MESH:D011528] (3014)   Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Malaria [MESH:D008288] (2175)   Malaria, Falciparum [MESH:D016778] (438)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Hepatoblastoma [MESH:D018197] (548)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Chondroma [MESH:D002812] (155)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Myxoma [MESH:D009232] (78)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibrosarcoma [MESH:D005354] (90)   Neurofibrosarcoma [MESH:D018319] (44)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyosarcoma [MESH:D007890] (977)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Leiomyosarcoma [MESH:D007890] (977)  Osteosarcoma [MESH:D012516] (2175)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Fibrosarcoma [MESH:D005354] (90)   Neurofibrosarcoma [MESH:D018319] (44)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Adenoma, Liver Cell [MESH:D018248] (685)  Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Thyroid cancer, papillary [MESH:C536915] (111)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma in Situ [MESH:D002278] (2111)  Carcinoma, Large Cell [MESH:D018287] (211)  Carcinoma, Lewis Lung [MESH:D018827] (248)  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)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Nerve Sheath Neoplasms [MESH:D018317] (365)   Neurofibrosarcoma [MESH:D018319] (44)  Neurofibroma [MESH:D009455] (177)   Neurofibrosarcoma [MESH:D018319] (44)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioblastoma [MESH:D018325] (395)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Pancreatic Neoplasms [MESH:D010190] (3820)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)  Pituitary Neoplasms [MESH:D010911] (981)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Laryngeal Neoplasms [MESH:D007822] (68)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Skin Neoplasms [MESH:D012878] (2992)   Dermatopathia pigmentosa reticularis [MESH:C535374] (38)  Sweat Gland Neoplasms [MESH:D013544] (46)  Thoracic Neoplasms [MESH:D013899] (6032)   Thymus Neoplasms [MESH:D013953] (247)  Heart Neoplasms [MESH:D006338] (47)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   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)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neoplasms, Experimental [MESH:D009374] (5218)   Carcinoma, Lewis Lung [MESH:D018827] (248)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplastic Processes [MESH:D009385] (5317)   Anaplasia [MESH:D000708] (348)  Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Precancerous Conditions [MESH:D011230] (2858)   Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Cartilage Diseases [MESH:D002357] (438)  Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Bone Diseases, Developmental [MESH:D001848] (3315)   Dwarfism [MESH:D004392] (778)  Dysostoses [MESH:D004413] (1019)  Osteochondrodysplasias [MESH:D010009] (2440)   Enchondromatosis [MESH:D004687] (170)  Chondrodysplasia Punctata [MESH:D002806] (108)   Chondrodysplasia Punctata, Rhizomelic [MESH:D018902] (53)   Rhizomelic chondrodysplasia punctata, type 3 [MESH:C537608] (26)  Osteosclerosis [MESH:D010026] (356)   Osteopetrosis [MESH:D010022] (318)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Osteitis Deformans [MESH:D010001] (287)   Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Spinal Diseases [MESH:D013122] (2485)   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)   Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)  Muscle Rigidity [MESH:D009127] (617)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Distal Myopathies [MESH:D049310] (178)   Distal myopathy, Nonaka type [MESH:C536816] (40)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 1 [MESH:C538348] (69)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Myositis, Inclusion Body [MESH:D018979] (103)   Inclusion body myopathy autosomal recessive [MESH:C538329] (40)  Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Microcephaly [MESH:D008831] (700)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 6 [MESH:C548084] (44)  Limb Deformities, Congenital [MESH:D017880] (1813)   Limb-mammary syndrome [MESH:C535903] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Split-Hand/Foot Malformation 4 [MESH:C565344] (46)  Split-Hand/Foot Malformation 6 [MESH:C567616] (29)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Cholangitis [MESH:D002761] (203)   Cholangitis, Sclerosing [MESH:D015209] (93)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Hirschsprung Disease [MESH:D006627] (361)  Digestive System Neoplasms [MESH:D004067] (7493)   Pancreatic Neoplasms [MESH:D010190] (3820)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Deglutition Disorders [MESH:D003680] (1538)   Esophageal Motility Disorders [MESH:D015154] (1489)   Gastroesophageal Reflux [MESH:D005764] (1465)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Gastroenteritis [MESH:D005759] (4066)   Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  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 Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Malabsorption Syndromes [MESH:D008286] (492)   Microvillus inclusion disease [MESH:C537470] (28)  Diarrhea 5, With Tufting Enteropathy, Congenital [MESH:C567703] (70)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   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)  Hepatic Veno-Occlusive Disease [MESH:D006504] (208)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatorenal Syndrome [MESH:D006530] (910)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Animal [MESH:D006520] (260)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatic Neoplasms [MESH:D010190] (3820)  Pancreatitis [MESH:D010195] (1924) 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)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Mouth Diseases [MESH:D009059] (4783)   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)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Propping Zerres syndrome [MESH:C538052] (46)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Propping Zerres syndrome [MESH:C538052] (46) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Bronchial Hyperreactivity [MESH:D016535] (1357)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Laryngeal Diseases [MESH:D007818] (215)   Laryngeal Neoplasms [MESH:D007822] (68)  Lung Diseases [MESH:D008171] (7249)   Hypertension, Pulmonary [MESH:D006976] (2000)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   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)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Dyspnea [MESH:D004417] (248)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Insufficiency [MESH:D012131] (841)   Hypoventilation [MESH:D007040] (360)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Laryngeal Neoplasms [MESH:D007822] (68)  Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Dementia, familial Danish [MESH:C538209] (26)  Deaf-Blind Disorders [MESH:D054062] (132)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Donnai-Barrow syndrome [MESH:C536390] (40)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Recessive 1b [MESH:C567213] (18)  Deafness, Autosomal Dominant 3B [MESH:C567215] (18)  Deafness, Autosomal Dominant 3A [MESH:C567277] (77)  Hearing Loss, Central [MESH:D006313] (140)   Jensen syndrome [MESH:C537568] (21)  Retrocochlear Diseases [MESH:D012181] (241)   Auditory Diseases, Central [MESH:D001304] (210)   Hearing Loss, Central [MESH:D006313] (140)   Jensen syndrome [MESH:C537568] (21)  Laryngeal Diseases [MESH:D007818] (211)   Laryngeal Neoplasms [MESH:D007822] (68)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Laryngeal Neoplasms [MESH:D007822] (68)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Autonomic Nervous System Diseases [MESH:D001342] (882)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Beta-Ureidopropionase Deficiency [MESH:C563210] (35)  Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Hypoxia, Brain [MESH:D002534] (134)  Auditory Diseases, Central [MESH:D001304] (210)   Hearing Loss, Central [MESH:D006313] (140)   Jensen syndrome [MESH:C537568] (21)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Homocystinuria [MESH:D006712] (93)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Hyperargininemia [MESH:D020162] (109)  Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Dementia, familial Danish [MESH:C538209] (26)  Episodic Ataxia, Type 6 [MESH:C567207] (70)  Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Cerebrovascular Disorders [MESH:D002561] (5542)   Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Jensen syndrome [MESH:C537568] (21)  Dementia, familial Danish [MESH:C538209] (26)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Lewy Body Disease [MESH:D020961] (1143)  Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  Alzheimer disease type 4 [MESH:C536596] (42)  Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)   Frontotemporal Dementia [MESH:D057180] (300)   Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Pick Disease of the Brain [MESH:D020774] (184)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Epilepsy [MESH:D004827] (6274)   Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsy, Generalized [MESH:D004829] (1431)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Spasms, Infantile [MESH:D013036] (468)  Seizures [MESH:D012640] (4502)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Seizures, Febrile [MESH:D003294] (229)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1250)   Hyperprolactinemia [MESH:D006966] (603)  Leukoencephalopathies [MESH:D056784] (1916)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Poliomyelitis [MESH:D011051] (56)  Myelitis [MESH:D009187] (69)   Poliomyelitis [MESH:D011051] (54)  Myelitis [MESH:D009187] (69)   Poliomyelitis [MESH:D011051] (54)  Prion Diseases [MESH:D017096] (488)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Beta-Ureidopropionase Deficiency [MESH:C563210] (35)  Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dystonic Disorders [MESH:D020821] (729)   Myoclonic dystonia [MESH:C536096] (245)  Juvenile-onset dystonia [MESH:C537704] (143)  Dystonia, Dopa-responsive [MESH:C538007] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Spinal Cord Diseases [MESH:D013118] (4376)   Poliomyelitis [MESH:D011051] (55)  Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Myelitis [MESH:D009187] (75)   Poliomyelitis [MESH:D011051] (54)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  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)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Jensen syndrome [MESH:C537568] (21)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Donnai-Barrow syndrome [MESH:C536390] (40)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Cobblestone Lissencephaly [MESH:D054222] (37)   Walker-Warburg Syndrome [MESH:D058494] (36)  Microcephaly [MESH:D008831] (700)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Neuronal Migration Disorders [MESH:D054081] (264)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  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)  Peripheral Nervous System Neoplasms [MESH:D010524] (287)   Nerve Sheath Neoplasms [MESH:D018317] (286)   Neurofibroma [MESH:D009455] (47)   Neurofibrosarcoma [MESH:D018319] (44)  Neurocutaneous Syndromes [MESH:D020752] (1230)   von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Rett Syndrome [MESH:D015518] (143)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Prion Diseases [MESH:D017096] (475)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  Alzheimer disease type 4 [MESH:C536596] (42)  Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)   Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Pain [MESH:D010146] (3875)  Reflex, Abnormal [MESH:D012021] (485)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Ataxia [MESH:D001259] (1138)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Cerebellar Ataxia [MESH:D002524] (542)   Dementia, familial Danish [MESH:C538209] (26)  Episodic Ataxia, Type 6 [MESH:C567207] (70)  Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Dystonia [MESH:D004421] (848)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Speech Disorders [MESH:D013064] (482)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)   Amnesia, Retrograde [MESH:D000648] (53)  Intellectual Disability [MESH:D008607] (3054)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Histidinemia [MESH:C538320] (87)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Williams Syndrome [MESH:D018980] (133)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Rett Syndrome [MESH:D015518] (143)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Apraxias [MESH:D001072] (118)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Paresis [MESH:D010291] (419)   Paraparesis [MESH:D020335] (77)   Paraparesis, Spastic [MESH:D020336] (70)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Seizures [MESH:D012640] (4514)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Sensation Disorders [MESH:D012678] (5011)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Dementia, familial Danish [MESH:C538209] (26)  Deaf-Blind Disorders [MESH:D054062] (132)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Donnai-Barrow syndrome [MESH:C536390] (40)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Recessive 1b [MESH:C567213] (18)  Deafness, Autosomal Dominant 3B [MESH:C567215] (18)  Deafness, Autosomal Dominant 3A [MESH:C567277] (77)  Hearing Loss, Central [MESH:D006313] (140)   Jensen syndrome [MESH:C537568] (21)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (501)   Blindness [MESH:D001766] (252)   Deaf-Blind Disorders [MESH:D054062] (132)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Neuromuscular Diseases [MESH:D009468] (7336)   Poliomyelitis [MESH:D011051] (55)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Diseases [MESH:D009135] (3538)   Erythrocyte Lactate Transporter Defect [MESH:C565449] (106)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Distal Myopathies [MESH:D049310] (178)   Distal myopathy, Nonaka type [MESH:C536816] (40)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  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)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 1 [MESH:C538348] (69)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Myositis, Inclusion Body [MESH:D018979] (103)   Inclusion body myopathy autosomal recessive [MESH:C538329] (40)  Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Peripheral Nervous System Neoplasms [MESH:D010524] (287)   Nerve Sheath Neoplasms [MESH:D018317] (286)   Neurofibroma [MESH:D009455] (47)   Neurofibrosarcoma [MESH:D018319] (44)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  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 Deprivation [MESH:D012892] (233)  Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)   Insomnia, Fatal Familial [MESH:D034062] (98)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Corneal Diseases [MESH:D003316] (1445)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Juvenile Epithelial of Meesmann [MESH:D053559] (12)  Eye Abnormalities [MESH:D005124] (1233)   Hay-Wells syndrome [MESH:C535847] (46)  Coloboma [MESH:D003103] (315)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Walker-Warburg Syndrome [MESH:D058494] (36)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Juvenile Epithelial of Meesmann [MESH:D053559] (12)  Leber Congenital Amaurosis [MESH:D057130] (157)   Leber Congenital Amaurosis 3 [MESH:C565814] (38)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Leber Congenital Amaurosis 3 [MESH:C565814] (38)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Lacrimal Duct Obstruction [MESH:D007767] (49)   Propping Zerres syndrome [MESH:C538052] (46)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Dementia, familial Danish [MESH:C538209] (26)  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)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Jensen syndrome [MESH:C537568] (21)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Refractive Errors [MESH:D012030] (457)   Myopia [MESH:D009216] (349)   Donnai-Barrow syndrome [MESH:C536390] (40)  Retinal Diseases [MESH:D012164] (3747)   Retinal Detachment [MESH:D012163] (1639)  Leber Congenital Amaurosis [MESH:D057130] (157)   Leber Congenital Amaurosis 3 [MESH:C565814] (38)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Leber Congenital Amaurosis 3 [MESH:C565814] (38)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Uveal Diseases [MESH:D014603] (2428)   Iris Diseases [MESH:D007499] (348)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Vision Disorders [MESH:D014786] (534)   Blindness [MESH:D001766] (259)   Deaf-Blind Disorders [MESH:D054062] (132)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Night Blindness [MESH:D009755] (76)   Oguchi disease [MESH:C537743] (22) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Urogenital Abnormalities [MESH:D014564] (2065)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Lipoprotein Glomerulopathy [MESH:C567089] (165)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Donnai-Barrow syndrome [MESH:C536390] (40)  Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  Albuminuria [MESH:D000419] (2394) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Uterine Diseases [MESH:D014591] (2479)   Endometrial Hyperplasia [MESH:D004714] (263)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Urogenital Abnormalities [MESH:D014564] (2043)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Lipoprotein Glomerulopathy [MESH:C567089] (165)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hydronephrosis [MESH:D006869] (956)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Donnai-Barrow syndrome [MESH:C536390] (40)  Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  Albuminuria [MESH:D000419] (2394)  Pregnancy Complications [MESH:D011248] (4768)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Abortion, Spontaneous [MESH:D000022] (2780)   Embryo Loss [MESH:D020964] (288)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316) 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)   Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 6 [MESH:C548084] (44)  Heart Diseases [MESH:D006331] (8614)   Cardiac Output, High [MESH:D016534] (123)  Heart Failure [MESH:D006333] (4058)  Pericardial Effusion [MESH:D010490] (1015)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  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, 1D [MESH:C563306] (50)  Cardiomyopathy, Dilated, 1p [MESH:C563690] (45)  Cardiomyopathy, Dilated, 1u [MESH:C566296] (56)  Cardiomyopathy, Dilated, 1V [MESH:C566856] (42)  Cardiomyopathies [MESH:D009202] (5331)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1D [MESH:C563306] (50)  Cardiomyopathy, Dilated, 1p [MESH:C563690] (45)  Cardiomyopathy, Dilated, 1u [MESH:C566296] (56)  Cardiomyopathy, Dilated, 1V [MESH:C566856] (42)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 2 [MESH:C566171] (50)  Cardiomyopathy, Restrictive [MESH:D002313] (94)   Cardiomyopathy, Familial Restrictive, 3 [MESH:C567316] (50)  Heart Defects, Congenital [MESH:D006330] (2443)   Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 6 [MESH:C548084] (44)  Heart Neoplasms [MESH:D006338] (47)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Aortic Stenosis, Supravalvular [MESH:D021921] (135)   Williams Syndrome [MESH:D018980] (133)  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)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  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)   Diabetic Angiopathies [MESH:D003925] (1984)  Hepatic Veno-Occlusive Disease [MESH:D006504] (208)  Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Carotid Stenosis [MESH:D016893] (174)  Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Cerebrovascular Disorders [MESH:D002561] (5541)   Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  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)  Embolism and Thrombosis [MESH:D016769] (3374)   Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  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)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Z. Exceptions (453)   Not Fully Specified [NFS] (453)  Hematologic Diseases [MESH:D006402] (6174)   Anemia [MESH:D000740] (3966)   Anemia, Hemolytic [MESH:D000743] (3083)   Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to [MESH:C565545] (88)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  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)  Blood Protein Disorders [MESH:D001796] (3051)   Hypergammaglobulinemia [MESH:D006942] (137)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic Syndromes [MESH:D009190] (2093)  Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Leukocyte Disorders [MESH:D007960] (2662)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Leukocytosis [MESH:D007964] (988)  Eosinophilia [MESH:D004802] (537)   Hypereosinophilic Syndrome [MESH:D017681] (119)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Thrombophilia [MESH:D019851] (592)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Lymphatic Diseases [MESH:D008206] (5167)   Thymus Neoplasms [MESH:D013953] (247)  Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Splenic Diseases [MESH:D013158] (1323)   Hypersplenism [MESH:D006971] (341) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Multiple [MESH:D000015] (3192)   Beta-Ureidopropionase Deficiency [MESH:C563210] (35)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Carney Complex [MESH:D056733] (45)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Deaf-Blind Disorders [MESH:D054062] (132)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Ectodermal Dysplasia [MESH:D004476] (938)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Naegeli syndrome [MESH:C538331] (38)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 6 [MESH:C548084] (44)  Chromosome Disorders [MESH:D025063] (2030)   Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Williams Syndrome [MESH:D018980] (133)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)  Eye Abnormalities [MESH:D005124] (1233)   Hay-Wells syndrome [MESH:C535847] (46)  Coloboma [MESH:D003103] (315)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Microcephaly [MESH:D008831] (700)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 6 [MESH:C548084] (44)  Limb Deformities, Congenital [MESH:D017880] (1813)   Limb-mammary syndrome [MESH:C535903] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Split-Hand/Foot Malformation 4 [MESH:C565344] (46)  Split-Hand/Foot Malformation 6 [MESH:C567616] (29)  Foot Deformities, Congenital [MESH:D005532] (538)   Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Hand Deformities, Congenital [MESH:D006228] (587)   Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Donnai-Barrow syndrome [MESH:C536390] (40)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Cobblestone Lissencephaly [MESH:D054222] (37)   Walker-Warburg Syndrome [MESH:D058494] (36)  Microcephaly [MESH:D008831] (700)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Neuronal Migration Disorders [MESH:D054081] (264)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Skin Abnormalities [MESH:D012868] (1723)   Carney Complex [MESH:D056733] (45)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Ectodermal Dysplasia [MESH:D004476] (958)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Naegeli syndrome [MESH:C538331] (38)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosis [MESH:D007057] (481)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Propping Zerres syndrome [MESH:C538052] (46)  Urogenital Abnormalities [MESH:D014564] (2064)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Dwarfism [MESH:D004392] (783)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 2 [MESH:C566171] (50)  Chromosome Disorders [MESH:D025063] (2030)   Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Williams Syndrome [MESH:D018980] (133)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Juvenile Epithelial of Meesmann [MESH:D053559] (12)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Leber Congenital Amaurosis 3 [MESH:C565814] (38)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Rett Syndrome [MESH:D015518] (143)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Rett Syndrome [MESH:D015518] (143)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Rett Syndrome [MESH:D015518] (143)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Metabolism, Inborn Errors [MESH:D008661] (6032)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Trimethylaminuria [MESH:C536561] (61)  Coumarin Resistance [MESH:C563039] (397)  Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutathione synthetase deficiency [MESH:C536835] (88)  Methylmalonic acidemia [MESH:C537358] (764)  Acidemia, isovaleric [MESH:C538167] (47)  Histidinemia [MESH:C538320] (87)  Methylmalonic Aciduria and Homocystinuria, CblF Type [MESH:C564747] (21)  Maple Syrup Urine Disease [MESH:D008375] (127)  Hyperhomocysteinemia [MESH:D020138] (1724)   Homocystinuria [MESH:D006712] (93)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Hyperargininemia [MESH:D020162] (109)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Homocystinuria [MESH:D006712] (93)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Hyperargininemia [MESH:D020162] (109)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease IC [MESH:C562805] (53)  Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Glycogen Storage Disease Type VI [MESH:D006013] (73)  Glycogen Storage Disease Type I [MESH:D005953] (140)   Glycogen Storage Disease IB [MESH:C562594] (53)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Chondrodysplasia Punctata, Rhizomelic [MESH:D018902] (53)   Rhizomelic chondrodysplasia punctata, type 3 [MESH:C537608] (26)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Beta-Ureidopropionase Deficiency [MESH:C563210] (35)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Donnai-Barrow syndrome [MESH:C536390] (40)  Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Walker-Warburg Syndrome [MESH:D058494] (36)  Distal Myopathies [MESH:D049310] (178)   Distal myopathy, Nonaka type [MESH:C536816] (40)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Skin Diseases, Genetic [MESH:D012873] (3456)   dowling-degos disease [MESH:C562924] (53)  Darier Disease [MESH:D007644] (125)  Dermatitis, Atopic [MESH:D003876] (2052)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ectodermal Dysplasia [MESH:D004476] (958)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Naegeli syndrome [MESH:C538331] (38)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Epidermolysis Bullosa [MESH:D004820] (259)   Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratosis palmoplantaris striata 1 [MESH:C536162] (54)  Keratosis palmoplantaris striata 3 [MESH:C536163] (48)  Naegeli syndrome [MESH:C538331] (38)  Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80)   Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)  Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Ichthyosis [MESH:D007057] (476)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Cartilage Diseases [MESH:D002357] (438)  Dermatomyositis [MESH:D003882] (1826)  Homocystinuria [MESH:D006712] (93)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 6 [MESH:C548084] (44)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  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)  Dermatitis, Occupational [MESH:D009783] (311)  Dermatitis, Seborrheic [MESH:D012628] (58)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)   Dermatopathia pigmentosa reticularis [MESH:C535374] (38)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Keratosis [MESH:D007642] (1941)   Darier Disease [MESH:D007644] (125)  Ichthyosis [MESH:D007057] (481)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratosis palmoplantaris striata 1 [MESH:C536162] (54)  Keratosis palmoplantaris striata 3 [MESH:C536163] (48)  Naegeli syndrome [MESH:C538331] (38)  Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80)   Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)  Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)  Nail Diseases [MESH:D009260] (203)   Dermatopathia pigmentosa reticularis [MESH:C535374] (38)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Pigmentation Disorders [MESH:D010859] (1215)   Propping Zerres syndrome [MESH:C538052] (46)  Hyperpigmentation [MESH:D017495] (523)   Dermatopathia pigmentosa reticularis [MESH:C535374] (38)  dowling-degos disease [MESH:C562924] (53)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Sebaceous Gland Diseases [MESH:D012625] (245)   Dermatitis, Seborrheic [MESH:D012628] (58)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Skin Abnormalities [MESH:D012868] (1709)   Pseudoxanthoma Elasticum [MESH:D011561] (115)  Ectodermal Dysplasia [MESH:D004476] (958)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Naegeli syndrome [MESH:C538331] (38)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosis [MESH:D007057] (481)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Dermatitis, Seborrheic [MESH:D012628] (58)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Skin Diseases, Genetic [MESH:D012873] (3481)   dowling-degos disease [MESH:C562924] (53)  Darier Disease [MESH:D007644] (125)  Dermatitis, Atopic [MESH:D003876] (2052)  Pseudoxanthoma Elasticum [MESH:D011561] (115)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ectodermal Dysplasia [MESH:D004476] (958)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Naegeli syndrome [MESH:C538331] (38)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Pachyonychia Congenita [MESH:D053549] (80)   Steatocystoma Multiplex [MESH:D062685] (56)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Keratosis palmoplantaris striata 1 [MESH:C536162] (54)  Keratosis palmoplantaris striata 3 [MESH:C536163] (48)  Naegeli syndrome [MESH:C538331] (38)  Keratoderma, Palmoplantar, Diffuse [MESH:D015776] (80)   Palmoplantar Keratoderma, Nonepidermolytic [MESH:C563422] (71)  Keratoderma, Palmoplantar, Epidermolytic [MESH:D053546] (75)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Bacterial [MESH:D017192] (156)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   dowling-degos disease [MESH:C562924] (53)  Dermatitis, Seborrheic [MESH:D012628] (58)   Ichthyosis hystrix, Curth Macklin type [MESH:C536088] (48)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Urticaria [MESH:D014581] (2668)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa, Junctional [MESH:D016109] (152)   Epidermolysis Bullosa, Junctional, Non-Herlitz Type [MESH:C562639] (150)  Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex, Autosomal Recessive [MESH:C563408] (38)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Skin Neoplasms [MESH:D012878] (2991)   Dermatopathia pigmentosa reticularis [MESH:C535374] (38)  Sweat Gland Neoplasms [MESH:D013544] (46)  Sweat Gland Diseases [MESH:D013543] (231)   Sweat Gland Neoplasms [MESH:D013544] (46)  Hidradenitis [MESH:D016575] (121)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Hypohidrosis [MESH:D007007] (47)   Naegeli syndrome [MESH:C538331] (38) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Z. Exceptions (817)   Not Fully Specified [NFS] (817)  Metabolic Diseases [MESH:D008659] (9025)   Iron Metabolism Disorders [MESH:D019189] (2139)  Metabolic Syndrome X [MESH:D024821] (2151)  Acid-Base Imbalance [MESH:D000137] (854)   Acidosis [MESH:D000138] (626)   Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Homocystinuria [MESH:D006712] (93)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Hyperargininemia [MESH:D020162] (109)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Colorectal Cancer, Hereditary Nonpolyposis, Type 8 [MESH:C567685] (70)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)  Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)  Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipid Metabolism, Inborn Errors [MESH:D008052] (461)  Dyslipidemias [MESH:D050171] (2428)   Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hypertriglyceridemia [MESH:D015228] (808)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Malabsorption Syndromes [MESH:D008286] (1869)   Microvillus inclusion disease [MESH:C537470] (28)  Diarrhea 5, With Tufting Enteropathy, Congenital [MESH:C567703] (70)  Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Trimethylaminuria [MESH:C536561] (61)  Coumarin Resistance [MESH:C563039] (397)  Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutathione synthetase deficiency [MESH:C536835] (88)  Methylmalonic acidemia [MESH:C537358] (764)  Acidemia, isovaleric [MESH:C538167] (47)  Histidinemia [MESH:C538320] (87)  Methylmalonic Aciduria and Homocystinuria, CblF Type [MESH:C564747] (21)  Maple Syrup Urine Disease [MESH:D008375] (127)  Hyperhomocysteinemia [MESH:D020138] (1724)   Homocystinuria [MESH:D006712] (93)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Hyperargininemia [MESH:D020162] (109)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Homocystinuria [MESH:D006712] (93)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Hyperargininemia [MESH:D020162] (109)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease IC [MESH:C562805] (53)  Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Glycogen Storage Disease Type VI [MESH:D006013] (73)  Glycogen Storage Disease Type I [MESH:D005953] (140)   Glycogen Storage Disease IB [MESH:C562594] (53)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Mucolipidoses [MESH:D009081] (78)   Microvillus inclusion disease [MESH:C537470] (28)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Chondrodysplasia Punctata, Rhizomelic [MESH:D018902] (53)   Rhizomelic chondrodysplasia punctata, type 3 [MESH:C537608] (26)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Beta-Ureidopropionase Deficiency [MESH:C563210] (35)  Lesch-Nyhan Syndrome [MESH:D007926] (129)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Donnai-Barrow syndrome [MESH:C536390] (40)  Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Mitochondrial Diseases [MESH:D028361] (2561)   Mitochondrial Phosphate Carrier Deficiency [MESH:C563665] (41)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  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)   Amyloidosis, Familial [MESH:D028226] (696)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Dementia, familial British [MESH:C538208] (26)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)   Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypokalemia [MESH:D007008] (1041)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)  Vitamin D Deficiency [MESH:D014808] (360)  Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Vitamin E Deficiency [MESH:D014811] (274)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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)   Dwarfism [MESH:D004392] (698)  Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)   Pigmented Nodular Adrenocortical Disease, Primary, 1 [MESH:C566469] (34)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Angiopathies [MESH:D003925] (1984)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)  Pituitary Neoplasms [MESH:D010911] (981)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1259)   Hyperprolactinemia [MESH:D006966] (603)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)  Hyperthyroidism [MESH:D006980] (1191)  Hypothyroidism [MESH:D007037] (496)   Thyroid Dyshormonogenesis 3 [MESH:C562769] (46)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Thyroiditis [MESH:D013966] (158)   Thyroiditis, Autoimmune [MESH:D013967] (149) C20. Immune System Diseases  C20. Immune System Diseases  Z. Exceptions (350)   Not Fully Specified [NFS] (350)  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Thyroiditis, Autoimmune [MESH:D013967] (79)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2695)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Dermatitis, Atopic [MESH:D003876] (2052)  Urticaria [MESH:D014581] (2668)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Common Variable Immunodeficiency [MESH:D017074] (70)  Lymphopenia [MESH:D008231] (990)  HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Bare Lymphocyte Syndrome, Type I [MESH:C565759] (101)  Immunoproliferative Disorders [MESH:D007160] (4761)   Hypergammaglobulinemia [MESH:D006942] (137)  Lymphoproliferative Disorders [MESH:D008232] (4734)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)  Hepatitis, Animal [MESH:D006520] (260)  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)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Donnai-Barrow syndrome [MESH:C536390] (40)  Alopecia [MESH:D000505] (1383)   Dermatopathia pigmentosa reticularis [MESH:C535374] (38)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Hypertrophy [MESH:D006984] (4476)   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)  Nails, Malformed [MESH:D009264] (184)   Propping Zerres syndrome [MESH:C538052] (46)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)   Colonic Polyps [MESH:D003111] (210)  Pathologic Processes [MESH:D010335] (9863)   Emphysema [MESH:D004646] (1096)  Gliosis [MESH:D005911] (1419)  Hyperammonemia [MESH:D022124] (322)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Leukocytosis [MESH:D007964] (978)  Necrosis [MESH:D009336] (4019)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Ulcer [MESH:D014456] (392)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Death [MESH:D003643] (1328)   Embryo Loss [MESH:D020964] (288)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Meier-Gorlin syndrome [MESH:C538012] (133)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Neoplastic Processes [MESH:D009385] (5317)   Anaplasia [MESH:D000708] (348)  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)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Cardiac Output, High [MESH:D016534] (123)  Edema [MESH:D004487] (3726)  Flushing [MESH:D005483] (506)  Hypergammaglobulinemia [MESH:D006942] (105)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Obesity, Morbid [MESH:D009767] (515)  Neurologic Manifestations [MESH:D009461] (8702)   Pain [MESH:D010146] (3869)  Reflex, Abnormal [MESH:D012021] (485)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Ataxia [MESH:D001259] (984)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Cerebellar Ataxia [MESH:D002524] (289)   Dementia, familial Danish [MESH:C538209] (26)  Episodic Ataxia, Type 6 [MESH:C567207] (70)  Dystonia [MESH:D004421] (848)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Apraxias [MESH:D001072] (114)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Speech Disorders [MESH:D013064] (482)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)   Amnesia, Retrograde [MESH:D000648] (53)  Intellectual Disability [MESH:D008607] (1476)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Histidinemia [MESH:C538320] (87)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Apraxias [MESH:D001072] (118)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Paresis [MESH:D010291] (419)   Paraparesis [MESH:D020335] (77)   Paraparesis, Spastic [MESH:D020336] (70)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Seizures [MESH:D012640] (4502)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Sensation Disorders [MESH:D012678] (5009)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)   Dementia, familial Danish [MESH:C538209] (26)  Deaf-Blind Disorders [MESH:D054062] (52)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Donnai-Barrow syndrome [MESH:C536390] (40)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Recessive 1b [MESH:C567213] (18)  Deafness, Autosomal Dominant 3B [MESH:C567215] (18)  Deafness, Autosomal Dominant 3A [MESH:C567277] (77)  Hearing Loss, Central [MESH:D006313] (140)   Jensen syndrome [MESH:C537568] (21)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (444)   Blindness [MESH:D001766] (178)   Deaf-Blind Disorders [MESH:D054062] (52)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Sleep Disorders [MESH:D012893] (1301)   Sleep Deprivation [MESH:D012892] (233)  Pain [MESH:D010146] (4511)   Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Diarrhea [MESH:D003967] (858)   Diarrhea, Infantile [MESH:D003968] (72)   Diarrhea 5, With Tufting Enteropathy, Congenital [MESH:C567703] (70)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Dyspnea [MESH:D004417] (248)  Hypoventilation [MESH:D007040] (359)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Skin Manifestations [MESH:D012877] (1250)   Purpura [MESH:D011693] (475)   Purpura, Thrombocytopenic [MESH:D011696] (237)   Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)  Urological Manifestations [MESH:D020924] (3532)   Lower Urinary Tract Symptoms [MESH:D059411] (612)   Urinary Bladder, Overactive [MESH:D053201] (530)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Dermatitis, Occupational [MESH:D009783] (311)  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)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Phencyclidine Abuse [MESH:D010623] (288)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Tobacco Use Disorder [MESH:D014029] (628)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   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)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Fractures, Bone [MESH:D050723] (597)   Fractures, Closed [MESH:D005596] (194)  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)   Heart Injuries [MESH:D006335] (82)  Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Nitroso Compounds [MESH:D009603] (680)   Nitrosamines [MESH:D009602] (261)   Dimethylnitrosamine [MESH:D004128] (10) 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)   Physical Examination [MESH:D010808] (1041)   Body Constitution [MESH:D001824] (450)   Body Weights and Measures [MESH:D001837] (448)   Body Size [MESH:D049628] (439)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Apraxias [MESH:D001072] (83)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Intellectual Disability [MESH:D008607] (1109)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Histidinemia [MESH:C538320] (87)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Psychomotor Disorders [MESH:D011596] (250)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Apraxias [MESH:D001072] (83)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Mental Disorders [MESH:D001523] (2063)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Cognition Disorders [MESH:D003072] (115)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dementia [MESH:D003704] (471)   Jensen syndrome [MESH:C537568] (21)  Dementia, familial Danish [MESH:C538209] (26)  Alzheimer Disease [MESH:D000544] (242)   Alzheimer disease type 2 [MESH:C536595] (165)  Alzheimer disease type 4 [MESH:C536596] (42)  Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Frontotemporal Lobar Degeneration [MESH:D057174] (112)   Frontotemporal Dementia [MESH:D057180] (109)   Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)  Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Mohr-Tranebjaerg syndrome [MESH:C535808] (21)  Histidinemia [MESH:C538320] (87)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65) G. Phenomena and Processes  G. Phenomena and Processes  Physiological Phenomena [MESH:D010829] (788)   Body Constitution [MESH:D001824] (453)   Body Weights and Measures [MESH:D001837] (444)   Body Size [MESH:D049628] (438)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)