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Current search: C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Nervous System Malformations [MESH:D009421] > Hereditary Sensory and Motor Neuropathy [MESH:D015417] > Charcot-Marie-Tooth Disease [MESH:D002607] > Charcot-Marie-Tooth Disease, Axonal, Type 2n [MESH:C567653] × Select any link to see items in a related category. more general categories    information about this item A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Syndactyly, type 3 [MESH:C538154] (192)  Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Meier-Gorlin syndrome [MESH:C538012] (133)  Face [MESH:D005145] (387)   Kniest dysplasia [MESH:C537207] (89)  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)  Spine [MESH:D013131] (258)   VACTERL hydrocephaly [MESH:C536521] (151)  Thorax [MESH:D013909] (62)   Ribs [MESH:D012272] (50)   Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Intestines [MESH:D007422] (271)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Lower Gastrointestinal Tract [MESH:D041741] (254)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Upper Gastrointestinal Tract [MESH:D041742] (236)   Esophagus [MESH:D004947] (200)   VACTERL hydrocephaly [MESH:C536521] (151)  Respiratory System [MESH:D012137] (321)   Trachea [MESH:D014132] (190)   VACTERL hydrocephaly [MESH:C536521] (151)  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   VACTERL hydrocephaly [MESH:C536521] (151)  Cardiovascular System [MESH:D002319] (1086)   Blood Vessels [MESH:D001808] (278)   Arteries [MESH:D001158] (173)   Retinal Artery [MESH:D012161] (78)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Retinal Vessels [MESH:D012171] (112)   Retinal Artery [MESH:D012161] (78)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Heart [MESH:D006321] (904)   Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Nervous System [MESH:D009420] (587)   Central Nervous System [MESH:D002490] (371)   Brain [MESH:D001921] (349)   Orofacial Cleft 1 [MESH:C566121] (81)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Meier-Gorlin syndrome [MESH:C538012] (133)  Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Uvea [MESH:D014602] (270)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Helicobacter Infections [MESH:D016481] (579)  Pasteurellaceae Infections [MESH:D016871] (348)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Staphylococcal Infections [MESH:D013203] (264)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Tuberculosis [MESH:D014376] (992)   Tuberculosis, Pulmonary [MESH:D014397] (678)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)  Eye Infections [MESH:D015817] (86)   Corneal Ulcer [MESH:D003320] (61) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Encephalitis [MESH:D004660] (226)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Herpesviridae Infections [MESH:D006566] (1944)   Sarcoma, Kaposi [MESH:D012514] (1578)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  RNA Virus Infections [MESH:D012327] (4215)   Arenaviridae Infections [MESH:D001117] (204)  Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Morbillivirus Infections [MESH:D018185] (87)   Measles [MESH:D008457] (83)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   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)  Slow Virus Diseases [MESH:D012897] (782)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  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)   Helminthiasis [MESH:D006373] (1644)   Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)  Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Cysts [MESH:D003560] (2625)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)  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, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Mixed Tumor, Mullerian [MESH:D018200] (64)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Lipoma [MESH:D008067] (159)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyosarcoma [MESH:D007890] (977)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Leiomyosarcoma [MESH:D007890] (977)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Kaposi [MESH:D012514] (1578)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  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)   Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Lewis Lung [MESH:D018827] (248)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Lobular [MESH:D018275] (305)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Cervical Intraepithelial Neoplasia [MESH:D018290] (56)  Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Lobular [MESH:D018275] (305)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  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)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  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)  Sarcoma, Kaposi [MESH:D012514] (1578)  Hemangioma [MESH:D006391] (690)   Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Digestive System Neoplasms [MESH:D004067] (7487)   Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Thyroid Neoplasms [MESH:D013964] (2040)  Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Eye Neoplasms [MESH:D005134] (400)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Thyroid Neoplasms [MESH:D013964] (2040)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Nose Neoplasms [MESH:D009669] (390)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Skin Neoplasms [MESH:D012878] (2992)   Sebaceous Gland Neoplasms [MESH:D012626] (154)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   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)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Precancerous Conditions [MESH:D011230] (2858)   Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Osteitis Deformans [MESH:D010001] (287)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromicric dysplasia [MESH:C535662] (520)  Marfan Syndrome [MESH:D008382] (646)  Proteus Syndrome [MESH:D016715] (152)  Dwarfism [MESH:D004392] (778)   Kniest dysplasia [MESH:C537207] (89)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 2 [MESH:C536017] (89)  Thanatophoric Dysplasia [MESH:D013796] (147)   Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)  Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Hypertelorism [MESH:D006972] (109)   Roberts Syndrome [MESH:C535687] (32)  Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Osteochondrodysplasias [MESH:D010009] (2440)   Spondyloepiphyseal dysplasia, congenita [MESH:C535788] (89)  Spondylometaphyseal dysplasia, Kozlowski type [MESH:C535797] (118)  Marshall syndrome [MESH:C536025] (52)  Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Kniest dysplasia [MESH:C537207] (89)  Strudwick syndrome [MESH:C537501] (89)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)  Osteoarthritis with Mild Chondrodysplasia [MESH:C565740] (89)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Fibrous Dysplasia of Bone [MESH:D005357] (737)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 2 [MESH:C536017] (89)  Thanatophoric Dysplasia [MESH:D013796] (147)   Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Bone Resorption [MESH:D001862] (2352)   Alveolar Bone Loss [MESH:D016301] (220)  Hyperostosis [MESH:D015576] (493)   Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Osteonecrosis [MESH:D010020] (539)   Femur Head Necrosis [MESH:D005271] (268)   Legg-Calve-Perthes Disease [MESH:D007873] (90)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)   Intervertebral disc disease [MESH:C535531] (514)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Cartilage Diseases [MESH:D002357] (438)   Keutel syndrome [MESH:C536167] (102)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Clubfoot [MESH:D003025] (79)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Jaw Diseases [MESH:D007571] (1601)   Mandibular Diseases [MESH:D008336] (395)  Maxillary Diseases [MESH:D008439] (354)  Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Stickler syndrome, type 1 [MESH:C537492] (89)  Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)   Osteoarthritis with Mild Chondrodysplasia [MESH:C565740] (89)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Muscle Rigidity [MESH:D009127] (617)  Myopathies, Structural, Congenital [MESH:D020914] (272)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Glycogen Storage Disease Type VII [MESH:D006014] (37)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2071)   Polymyositis [MESH:D017285] (2007)  Myotonic Disorders [MESH:D020967] (138)   Dystrophia myotonica 2 [MESH:C538009] (34)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Roberts Syndrome [MESH:C535687] (32)  Marshall syndrome [MESH:C536025] (52)  Oculodentodigital Dysplasia [MESH:C563160] (192)  LIG4 Syndrome [MESH:C564694] (24)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  LEOPARD Syndrome [MESH:D044542] (299)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Hypertelorism [MESH:D006972] (109)   Roberts Syndrome [MESH:C535687] (32)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mowat-Wilson syndrome [MESH:C536990] (37)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  VACTERL hydrocephaly [MESH:C536521] (151)  Polydactyly [MESH:D017689] (318)  Proteus Syndrome [MESH:D016715] (152)  Ectromelia [MESH:D004480] (108)   Roberts Syndrome [MESH:C535687] (32)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Clubfoot [MESH:D003025] (79)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Thanatophoric Dysplasia [MESH:D013796] (147)   Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)   Osteoarthritis with Mild Chondrodysplasia [MESH:C565740] (89) 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)   Cholangitis [MESH:D002761] (203)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Hirschsprung Disease [MESH:D006627] (361)   Mowat-Wilson syndrome [MESH:C536990] (37)  Digestive System Neoplasms [MESH:D004067] (7493)   Gastrointestinal Neoplasms [MESH:D005770] (6460)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  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)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Intestinal Perforation [MESH:D007416] (471)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)   Mowat-Wilson syndrome [MESH:C536990] (37)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Malabsorption Syndromes [MESH:D008286] (492)   Celiac Disease [MESH:D002446] (340)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Peritoneal Diseases [MESH:D010532] (1119)   Peritoneal Fibrosis [MESH:D056627] (488) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Mandibular Diseases [MESH:D008336] (450)  Maxillary Diseases [MESH:D008439] (354)  Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 2 [MESH:C566394] (23)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Oral Ulcer [MESH:D019226] (488)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 1 [MESH:C566121] (81)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 1 [MESH:C566121] (81)  Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Periodontal Diseases [MESH:D010510] (1001)   Periodontal Atrophy [MESH:D055093] (225)   Alveolar Bone Loss [MESH:D016301] (220)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 2 [MESH:C566394] (23)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 1 [MESH:C566121] (81)  Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Respiratory System Abnormalities [MESH:D015619] (243)  Thoracic Diseases [MESH:D013896] (81)  Bronchial Diseases [MESH:D001982] (4382)   Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Hypertension, Pulmonary [MESH:D006976] (2000)  Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   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)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Neoplasms [MESH:D008175] (6012)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)   Hyaline Membrane Disease [MESH:D006819] (93)   Kniest dysplasia [MESH:C537207] (89)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Hyperventilation [MESH:D006985] (654)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)   Hyaline Membrane Disease [MESH:D006819] (93)   Kniest dysplasia [MESH:C537207] (89)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Nose Neoplasms [MESH:D009669] (390)  Lung Neoplasms [MESH:D008175] (6013)   Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sudden [MESH:D003639] (56)  Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Conductive [MESH:D006314] (134)   Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Marshall syndrome [MESH:C536025] (52)  Stickler syndrome, type 1 [MESH:C537492] (89)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Nose Neoplasms [MESH:D009669] (390)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Restless Legs Syndrome [MESH:D012148] (379)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Familial porencephaly [MESH:C536850] (77)  Brain Injuries [MESH:D001930] (3429)  Brain Neoplasms [MESH:D001932] (2764)  Hypoxia, Brain [MESH:D002534] (134)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease, Secondary [MESH:D010302] (327)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  Cerebrovascular Disorders [MESH:D002561] (5542)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)   Migraine without Aura [MESH:D020326] (408)  Hydrocephalus [MESH:D006849] (276)   VACTERL hydrocephaly [MESH:C536521] (151)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)   VACTERL hydrocephaly [MESH:C536521] (151)  Leukoencephalopathies [MESH:D056784] (1916)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Encephalitis [MESH:D004660] (226)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Encephalitis [MESH:D004660] (351)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Meningitis [MESH:D008581] (1506)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Movement Disorders [MESH:D009069] (4823)   Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Dystonic Disorders [MESH:D020821] (729)   Dystonia, Dopa-responsive [MESH:C538007] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease, Secondary [MESH:D010302] (327)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Chronobiology Disorders [MESH:D021081] (970)   Smith-Magenis Syndrome [MESH:D058496] (19)   Potocki-Lupski syndrome [MESH:C538355] (17)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Vestibulocochlear Nerve Diseases [MESH:D000160] (111)   Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Axonal, Type 2n [MESH:C567653] (33)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Norman Roberts lissencephaly syndrome [MESH:C537848] (58)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mowat-Wilson syndrome [MESH:C536990] (37)  Neural Tube Defects [MESH:D009436] (2143)   Meningomyelocele [MESH:D008591] (100)  Spinal Dysraphism [MESH:D016135] (1025)  Anencephaly [MESH:D000757] (120)   Neural tube defect, folate-sensitive [MESH:C536409] (111)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neurodegenerative Diseases [MESH:D019636] (6613)   Familial apoceruloplasmin deficiency [MESH:C536004] (211)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hepatolenticular Degeneration [MESH:D006527] (473)  Rett Syndrome [MESH:D015518] (143)  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 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Axonal, Type 2n [MESH:C567653] (33)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Ataxia [MESH:D001259] (1138)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Psychomotor Agitation [MESH:D011595] (167)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)   Amnesia, Retrograde [MESH:D000648] (53)  Intellectual Disability [MESH:D008607] (3054)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Mental Retardation, X-Linked 63 [MESH:C564522] (64)  Adrenoleukodystrophy [MESH:D000326] (1348)  Rett Syndrome [MESH:D015518] (143)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  Psychomotor Disorders [MESH:D011596] (576)   Psychomotor Agitation [MESH:D011595] (167)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Paralysis [MESH:D010243] (2043)   Hemiplegia [MESH:D006429] (184)   Familial porencephaly [MESH:C536850] (77)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sudden [MESH:D003639] (56)  Deafness [MESH:D003638] (623)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Conductive [MESH:D006314] (134)   Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Marshall syndrome [MESH:C536025] (52)  Stickler syndrome, type 1 [MESH:C537492] (89)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Diseases [MESH:D009135] (3538)   Myopathies, Structural, Congenital [MESH:D020914] (272)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Myositis [MESH:D009220] (2069)   Polymyositis [MESH:D017285] (2007)  Myotonic Disorders [MESH:D020967] (138)   Dystrophia myotonica 2 [MESH:C538009] (34)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  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 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Axonal, Type 2n [MESH:C567653] (33)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Restless Legs Syndrome [MESH:D012148] (379)  Parasomnias [MESH:D020447] (453)   Restless Legs Syndrome [MESH:D012148] (379)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76)  Conjunctival Diseases [MESH:D003229] (273)   Pemphigoid, Benign Mucous Membrane [MESH:D010390] (61)  Corneal Diseases [MESH:D003316] (1445)   Keratoconus [MESH:D007640] (121)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Keratitis [MESH:D007634] (168)   Corneal Ulcer [MESH:D003320] (61)  Eye Abnormalities [MESH:D005124] (1233)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Stickler Syndrome, Type I, Nonsyndromic Ocular [MESH:C563709] (89)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Retinitis Pigmentosa [MESH:D012174] (414)   Cone-Rod Dystrophy 10 [MESH:C564597] (30)  Retinitis Pigmentosa 35 [MESH:C565206] (30)  Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Eye Hemorrhage [MESH:D005130] (94)   Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Eye Infections [MESH:D015817] (110)   Corneal Ulcer [MESH:D003320] (61)  Eye Neoplasms [MESH:D005134] (413)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Marshall syndrome [MESH:C536025] (52)  Cataract, Pulverulent, Juvenile-Onset [MESH:C565703] (69)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma 3, Primary Congenital, D [MESH:C567765] (31)  Glaucoma, Angle-Closure [MESH:D015812] (73)  Glaucoma, Open-Angle [MESH:D005902] (1281)   Glaucoma, Primary Open Angle [MESH:C562750] (466)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)  Refractive Errors [MESH:D012030] (457)   Anisometropia [MESH:D015858] (152)  Myopia [MESH:D009216] (349)   Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Degeneration [MESH:D012162] (2386)   Hyaloideoretinal degeneration of Wagner [MESH:C536075] (135)  Macular Degeneration [MESH:D008268] (995)   Stargardt disease 4 [MESH:C535521] (63)  Fundus Dystrophy, Pseudoinflammatory, Of Sorsby [MESH:C564992] (121)  Macular Degeneration, Age-Related, 4 [MESH:C565196] (67)  Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Cone-Rod Dystrophy 10 [MESH:C564597] (30)  Retinitis Pigmentosa 35 [MESH:C565206] (30)  Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Retinal Detachment [MESH:D012163] (1639)   Stickler syndrome, type 1 [MESH:C537492] (89)  Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784)  Vitreous Detachment [MESH:D020255] (53)   Stickler syndrome, type 2 [MESH:C537493] (52) 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)   Prostate cancer, familial [MESH:C537243] (264)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Asthenozoospermia [MESH:D053627] (298)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)  Penile Induration [MESH:D010411] (495)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)  Urogenital Abnormalities [MESH:D014564] (2065)   Cryptorchidism [MESH:D003456] (215)  Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   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)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  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)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal tubular acidosis, distal, autosomal recessive [MESH:C537758] (48)  Renal Tubular Acidosis, Distal, With Hemolytic Anemia [MESH:C566910] (45)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Ureteral Obstruction [MESH:D014517] (575)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Urination Disorders [MESH:D014555] (3598)   Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Uterine Diseases [MESH:D014591] (2479)   Endometrial Hyperplasia [MESH:D004714] (263)  Uterine Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urogenital Abnormalities [MESH:D014564] (2043)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   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)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  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)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal tubular acidosis, distal, autosomal recessive [MESH:C537758] (48)  Renal Tubular Acidosis, Distal, With Hemolytic Anemia [MESH:C566910] (45)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Ureteral Obstruction [MESH:D014517] (575)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Urination Disorders [MESH:D014555] (3598)   Urinary Retention [MESH:D016055] (411)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Pregnancy Complications [MESH:D011248] (4768)   Diabetes, Gestational [MESH:D016640] (1157)  Fetal Death [MESH:D005313] (464)  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)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Abruptio Placentae [MESH:D000037] (430)  Fetal Membranes, Premature Rupture [MESH:D005322] (356)  Obstetric Labor, Premature [MESH:D007752] (1316)  Placenta Diseases [MESH:D010922] (1781)   Abruptio Placentae [MESH:D000037] (430)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   VACTERL hydrocephaly [MESH:C536521] (151)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Vascular Malformations [MESH:D054079] (1098)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Pericardial Effusion [MESH:D010490] (1015)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Cardiac Complexes, Premature [MESH:D005117] (429)   Ventricular Premature Complexes [MESH:D018879] (418)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 11 [MESH:C567513] (48)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Cardiomegaly [MESH:D006332] (4081)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1w [MESH:C566954] (66)  Cardiomyopathies [MESH:D009202] (5331)   Endomyocardial Fibrosis [MESH:D004719] (521)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1w [MESH:C566954] (66)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 15 [MESH:C567681] (66)  Heart Defects, Congenital [MESH:D006330] (2443)   VACTERL hydrocephaly [MESH:C536521] (151)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   Keutel syndrome [MESH:C536167] (102)  LEOPARD Syndrome [MESH:D044542] (299)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Microvascular Angina [MESH:D017566] (44)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Coronary Thrombosis [MESH:D003328] (255)  Coronary Vasospasm [MESH:D003329] (533)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Valve, Calcification of [MESH:C562942] (655)  Pulmonary Valve Stenosis [MESH:D011666] (109)   Keutel syndrome [MESH:C536167] (102)  Vascular Diseases [MESH:D014652] (8691)   Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Coronary Aneurysm [MESH:D003323] (204)  Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  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)  Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebrovascular Disorders [MESH:D002561] (5541)   Brain Ischemia [MESH:D002545] (4873)   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)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebral Arterial Diseases [MESH:D002539] (2440)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)  Thrombosis [MESH:D013927] (3101)   Coronary Thrombosis [MESH:D003328] (255)  Venous Thrombosis [MESH:D020246] (1141)  Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Pregnancy-Induced [MESH:D046110] (397)  Hypertension, Renal [MESH:D006977] (698)   Hypertension, Renovascular [MESH:D006978] (365)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Microvascular Angina [MESH:D017566] (44)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Coronary Thrombosis [MESH:D003328] (255)  Coronary Vasospasm [MESH:D003329] (533)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Raynaud Disease [MESH:D011928] (490)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784)  Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Z. Exceptions (453)   Not Fully Specified [NFS] (453)  Hematologic Diseases [MESH:D006402] (6174)   Adenosine Triphosphate, Elevated, Of Erythrocytes [MESH:C566310] (78)  Thrombophilia [MESH:D019851] (592)  Anemia [MESH:D000740] (3966)   Anemia, Neonatal [MESH:D000751] (20)  Anemia, Sideroblastic [MESH:D000756] (636)  Anemia, Hemolytic [MESH:D000743] (3083)   Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to [MESH:C565557] (312)  Renal Tubular Acidosis, Distal, With Hemolytic Anemia [MESH:C566910] (45)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Elliptocytosis, Hereditary [MESH:D004612] (95)   Pyropoikilocytosis, Hereditary [MESH:C563004] (21)  Elliptocytosis 2 [MESH:C565058] (21)  Spherocytosis, Hereditary [MESH:D013103] (137)   Spherocytosis, Type 1 [MESH:C567159] (21)  Spherocytosis, Type 4 [MESH:C567208] (45)  Spherocytosis, Type 3 [MESH:C567489] (21)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Blood Coagulation Disorders [MESH:D001778] (1828)   Blood Coagulation Disorders, Inherited [MESH:D025861] (720)  Thrombocythemia, Essential [MESH:D013920] (707)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Agammaglobulinemia [MESH:D000361] (156)  Hypergammaglobulinemia [MESH:D006942] (137)  Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic Syndromes [MESH:D009190] (2093)   Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Anemia, Sideroblastic [MESH:D000756] (636)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  alpha-Thalassemia [MESH:D017085] (192)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Hemorrhagic Disorders [MESH:D006474] (3359)   Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328)  Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Leukocyte Disorders [MESH:D007960] (2662)   Leukostasis [MESH:D018921] (769)  Eosinophilia [MESH:D004802] (537)   Reticuloendotheliosis, familial, with eosinophilia [MESH:C538564] (44)  Hypereosinophilic Syndrome [MESH:D017681] (119)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Combined Cellular And Humoral Immune Defects With Granulomas [MESH:C567115] (25)  Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Polycythemia [MESH:D011086] (412)   Polycythemia, primary familial and congenital [MESH:C536842] (45)  Lymphatic Diseases [MESH:D008206] (5167)   Splenic Diseases [MESH:D013158] (1323)  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 C [MESH:D052556] (103)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Agammaglobulinemia [MESH:D000361] (156)  Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Keutel syndrome [MESH:C536167] (102)  Bloom Syndrome [MESH:D001816] (107)  Down Syndrome [MESH:D004314] (1287)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Proteus Syndrome [MESH:D016715] (152)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Ectodermal Dysplasia [MESH:D004476] (938)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Smith-Magenis Syndrome [MESH:D058496] (19)   Potocki-Lupski syndrome [MESH:C538355] (17)  Waardenburg Syndrome [MESH:D014849] (243)   ABCD syndrome [MESH:C535334] (143)  Abnormalities, Severe Teratoid [MESH:D009008] (124)   Anencephaly [MESH:D000757] (120)   Neural tube defect, folate-sensitive [MESH:C536409] (111)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   VACTERL hydrocephaly [MESH:C536521] (151)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 11 [MESH:C567513] (48)  Vascular Malformations [MESH:D054079] (1108)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1018)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Smith-Magenis Syndrome [MESH:D058496] (19)   Potocki-Lupski syndrome [MESH:C538355] (17)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)   Mowat-Wilson syndrome [MESH:C536990] (37)  Eye Abnormalities [MESH:D005124] (1233)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Roberts Syndrome [MESH:C535687] (32)  Marshall syndrome [MESH:C536025] (52)  Oculodentodigital Dysplasia [MESH:C563160] (192)  LIG4 Syndrome [MESH:C564694] (24)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  LEOPARD Syndrome [MESH:D044542] (299)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Hypertelorism [MESH:D006972] (109)   Roberts Syndrome [MESH:C535687] (32)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mowat-Wilson syndrome [MESH:C536990] (37)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  VACTERL hydrocephaly [MESH:C536521] (151)  Polydactyly [MESH:D017689] (318)  Proteus Syndrome [MESH:D016715] (152)  Ectromelia [MESH:D004480] (108)   Roberts Syndrome [MESH:C535687] (32)  Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Clubfoot [MESH:D003025] (79)  Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Thanatophoric Dysplasia [MESH:D013796] (147)   Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)  Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Central Nervous System Cysts [MESH:D020863] (57)   Arachnoid Cysts [MESH:D016080] (50)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Axonal, Type 2n [MESH:C567653] (33)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Norman Roberts lissencephaly syndrome [MESH:C537848] (58)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mowat-Wilson syndrome [MESH:C536990] (37)  Neural Tube Defects [MESH:D009436] (2143)   Meningomyelocele [MESH:D008591] (100)  Spinal Dysraphism [MESH:D016135] (1025)  Anencephaly [MESH:D000757] (120)   Neural tube defect, folate-sensitive [MESH:C536409] (111)  Skin Abnormalities [MESH:D012868] (1723)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Micrognathism [MESH:D008844] (230)   Meier-Gorlin syndrome [MESH:C538012] (133)  Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 1 [MESH:C566121] (81)  Cleft Palate [MESH:D002972] (1330)   Kniest dysplasia [MESH:C537207] (89)  Orofacial Cleft 1 [MESH:C566121] (81)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Urogenital Abnormalities [MESH:D014564] (2064)   Cryptorchidism [MESH:D003456] (215)  Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Cystic Fibrosis [MESH:D003550] (760)  Marfan Syndrome [MESH:D008382] (646)  Werner Syndrome [MESH:D014898] (88)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Elliptocytosis, Hereditary [MESH:D004612] (95)   Pyropoikilocytosis, Hereditary [MESH:C563004] (21)  Elliptocytosis 2 [MESH:C565058] (21)  Spherocytosis, Hereditary [MESH:D013103] (137)   Spherocytosis, Type 1 [MESH:C567159] (21)  Spherocytosis, Type 4 [MESH:C567208] (45)  Spherocytosis, Type 3 [MESH:C567489] (21)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  alpha-Thalassemia [MESH:D017085] (176)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 15 [MESH:C567681] (66)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Smith-Magenis Syndrome [MESH:D058496] (19)   Potocki-Lupski syndrome [MESH:C538355] (17)  Dwarfism [MESH:D004392] (783)   Kniest dysplasia [MESH:C537207] (89)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 2 [MESH:C536017] (89)  Thanatophoric Dysplasia [MESH:D013796] (147)   Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Stickler Syndrome, Type I, Nonsyndromic Ocular [MESH:C563709] (89)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Corneal Dystrophy, Congenital Stromal [MESH:C566452] (90)  Retinitis Pigmentosa [MESH:D012174] (442)   Cone-Rod Dystrophy 10 [MESH:C564597] (30)  Retinitis Pigmentosa 35 [MESH:C565206] (30)  Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Combined Cellular And Humoral Immune Defects With Granulomas [MESH:C567115] (25)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Mental Retardation, X-Linked 63 [MESH:C564522] (64)  Adrenoleukodystrophy [MESH:D000326] (1348)  Rett Syndrome [MESH:D015518] (143)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  alpha-Thalassemia [MESH:D017085] (192)   ATR-X syndrome [MESH:C538258] (59)  Alpha-Thalassemia Myelodysplasia Syndrome [MESH:C563023] (59)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hepatolenticular Degeneration [MESH:D006527] (473)  Rett Syndrome [MESH:D015518] (143)  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 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Axonal, Type 2n [MESH:C567653] (33)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  ATR-X syndrome [MESH:C538258] (59)  Mental Retardation, X-Linked 63 [MESH:C564522] (64)  Adrenoleukodystrophy [MESH:D000326] (1348)  Rett Syndrome [MESH:D015518] (143)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107)  Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Hyperhomocysteinemia [MESH:D020138] (1724)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease Type VII [MESH:D006014] (37)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  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)   Cholesterol Ester Storage Disease [MESH:D015217] (49)   Wolman Disease [MESH:D015223] (48)   Lysosomal acid lipase deficiency [MESH:C531854] (46)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Lysosomal Storage Diseases [MESH:D016464] (761)   Cholesterol Ester Storage Disease [MESH:D015217] (49)   Wolman Disease [MESH:D015223] (48)   Lysosomal acid lipase deficiency [MESH:C531854] (46)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, type 3 [MESH:C537248] (20)  Hypophosphatasia [MESH:D007014] (142)   Hypophosphatasia, Childhood [MESH:C562440] (137)  Hypophosphatasia, Infantile [MESH:C562646] (137)  Hypophosphatasia, Adult [MESH:C562647] (137)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal tubular acidosis, distal, autosomal recessive [MESH:C537758] (48)  Renal Tubular Acidosis, Distal, With Hemolytic Anemia [MESH:C566910] (45)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Muscular Dystrophies [MESH:D009136] (1597)   Glycogen Storage Disease Type VII [MESH:D006014] (37)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Anemia, Neonatal [MESH:D000751] (20)  Asphyxia Neonatorum [MESH:D001238] (1648)  Cystic Fibrosis [MESH:D003550] (760)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Infant, Premature, Diseases [MESH:D007235] (1292)   Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)   Hyaline Membrane Disease [MESH:D006819] (93)   Kniest dysplasia [MESH:C537207] (89)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Reticuloendotheliosis, familial, with eosinophilia [MESH:C538564] (44)  Combined Cellular And Humoral Immune Defects With Granulomas [MESH:C567115] (25)  Thanatophoric Dysplasia [MESH:D013796] (147)   Platyspondylic Lethal Skeletal Dysplasia, Torrance Type [MESH:C563627] (89)  Wolman Disease [MESH:D015223] (48)   Lysosomal acid lipase deficiency [MESH:C531854] (46) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Stickler syndrome, type 1 [MESH:C537492] (89)  Stickler syndrome, type 2 [MESH:C537493] (52)  Marfan Syndrome [MESH:D008382] (646)  Penile Induration [MESH:D010411] (495)  Scleroderma, Systemic [MESH:D012595] (199)  Cartilage Diseases [MESH:D002357] (438)   Keutel syndrome [MESH:C536167] (102)  Collagen Diseases [MESH:D003095] (1267)   Kniest dysplasia [MESH:C537207] (89)  Keloid [MESH:D007627] (1111)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Exanthema [MESH:D005076] (301)  Lipomatosis [MESH:D008068] (182)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Scleroderma, Systemic [MESH:D012595] (199)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Sebaceous Gland Diseases [MESH:D012625] (245)   Sebaceous Gland Neoplasms [MESH:D012626] (154)  Skin Abnormalities [MESH:D012868] (1709)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome type 3 [MESH:C536196] (142)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Pemphigoid, Benign Mucous Membrane [MESH:D010390] (61)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Skin Neoplasms [MESH:D012878] (2991)   Sebaceous Gland Neoplasms [MESH:D012626] (154) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Metabolic Syndrome X [MESH:D024821] (2151)  Acid-Base Imbalance [MESH:D000137] (854)   Acidosis [MESH:D000138] (626)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal tubular acidosis, distal, autosomal recessive [MESH:C537758] (48)  Renal Tubular Acidosis, Distal, With Hemolytic Anemia [MESH:C566910] (45)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Keutel syndrome [MESH:C536167] (102)  Aortic Valve, Calcification of [MESH:C562942] (655)  Vascular Calcification [MESH:D061205] (138)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Bloom Syndrome [MESH:D001816] (107)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Werner Syndrome [MESH:D014898] (88)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Reticuloendotheliosis, familial, with eosinophilia [MESH:C538564] (44)  Combined Cellular And Humoral Immune Defects With Granulomas [MESH:C567115] (25)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Iron Metabolism Disorders [MESH:D019189] (2139)   Familial apoceruloplasmin deficiency [MESH:C536004] (211)  Anemia, Iron-Deficiency [MESH:D018798] (547)  Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, type 3 [MESH:C537248] (20)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipomatosis [MESH:D008068] (182)  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)  Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Lipidoses [MESH:D008064] (1655)   Cholesterol Ester Storage Disease [MESH:D015217] (49)   Wolman Disease [MESH:D015223] (48)   Lysosomal acid lipase deficiency [MESH:C531854] (46)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Malabsorption Syndromes [MESH:D008286] (1869)   Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Hyperhomocysteinemia [MESH:D020138] (1724)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease Type VII [MESH:D006014] (37)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  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)   Cholesterol Ester Storage Disease [MESH:D015217] (49)   Wolman Disease [MESH:D015223] (48)   Lysosomal acid lipase deficiency [MESH:C531854] (46)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Lysosomal Storage Diseases [MESH:D016464] (761)   Cholesterol Ester Storage Disease [MESH:D015217] (49)   Wolman Disease [MESH:D015223] (48)   Lysosomal acid lipase deficiency [MESH:C531854] (46)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, type 3 [MESH:C537248] (20)  Hypophosphatasia [MESH:D007014] (142)   Hypophosphatasia, Childhood [MESH:C562440] (137)  Hypophosphatasia, Infantile [MESH:C562646] (137)  Hypophosphatasia, Adult [MESH:C562647] (137)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal tubular acidosis, distal, autosomal recessive [MESH:C537758] (48)  Renal Tubular Acidosis, Distal, With Hemolytic Anemia [MESH:C566910] (45)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Mitochondrial Diseases [MESH:D028361] (2561)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Dwarfism [MESH:D004392] (698)   Kniest dysplasia [MESH:C537207] (89)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Thyroid Neoplasms [MESH:D013964] (2040)  Ovarian Neoplasms [MESH:D010051] (3275)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)  Hypogonadism [MESH:D007006] (1123)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Ovarian Neoplasms [MESH:D010051] (3281)   Hereditary Breast and Ovarian Cancer Syndrome [MESH:D061325] (143)  Testicular Diseases [MESH:D013733] (777)   Cryptorchidism [MESH:D003456] (215)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040)  Thyrotoxicosis [MESH:D013971] (93)  Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)  Thyrotoxicosis [MESH:D013971] (93) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Graves Disease [MESH:D006111] (278)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Hypersensitivity [MESH:D006967] (5873)   Immune Complex Diseases [MESH:D007105] (782)  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)  Urticaria [MESH:D014581] (2668)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Food Hypersensitivity [MESH:D005512] (608)   Peanut Hypersensitivity [MESH:D021183] (572)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell -Negative, NK Cell-Positive [MESH:C563311] (25)  Neutrophil Immunodeficiency Syndrome [MESH:C564275] (47)  LIG4 Syndrome [MESH:C564694] (24)  MYD88 Deficiency [MESH:C567379] (79)  Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Agammaglobulinemia [MESH:D000361] (156)  Common Variable Immunodeficiency [MESH:D017074] (70)  HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Granulomatous Disease, Chronic [MESH:D006105] (404)   Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111)  Combined Cellular And Humoral Immune Defects With Granulomas [MESH:C567115] (25)  Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Reticuloendotheliosis, familial, with eosinophilia [MESH:C538564] (44)  Combined Cellular And Humoral Immune Defects With Granulomas [MESH:C567115] (25)  Immunoproliferative Disorders [MESH:D007160] (4761)   Hypergammaglobulinemia [MESH:D006942] (137)  Lymphoproliferative Disorders [MESH:D008232] (4734)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Plaque, Atherosclerotic [MESH:D058226] (696)  Ventricular Remodeling [MESH:D020257] (686)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Hernia [MESH:D006547] (2825)   Hernia, Abdominal [MESH:D046449] (208)   Hernia, Inguinal [MESH:D006552] (111)  Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Hypertrophy [MESH:D006984] (4476)   Splenomegaly [MESH:D013163] (1258)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Prolapse [MESH:D011391] (60)   Pelvic Organ Prolapse [MESH:D056887] (59)  Pathologic Processes [MESH:D010335] (9863)   Hemolysis [MESH:D006461] (280)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  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)  Cardiac Complexes, Premature [MESH:D005117] (429)   Ventricular Premature Complexes [MESH:D018879] (418)  Long QT Syndrome [MESH:D008133] (691)   Long Qt Syndrome 11 [MESH:C567513] (48)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Chromosome Aberrations [MESH:D002869] (2352)   Chromosome Breakage [MESH:D019457] (139)  Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Death [MESH:D003643] (1328)   Embryo Loss [MESH:D020964] (288)  Fetal Death [MESH:D005313] (464)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Facies [MESH:D019066] (738)   Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Macrocephaly Autism Syndrome [MESH:C565342] (151)  Fibrosis [MESH:D005355] (3133)   Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Genomic Instability [MESH:D042822] (184)   Microsatellite Instability [MESH:D053842] (141)  Growth Disorders [MESH:D006130] (2438)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Meier-Gorlin syndrome [MESH:C538012] (133)  LIG4 Syndrome [MESH:C564694] (24)  Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Eye Hemorrhage [MESH:D005130] (94)   Retinal Hemorrhage [MESH:D012166] (84)   Brain Small Vessel Disease with Hemorrhage [MESH:C564372] (77)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)  Necrosis [MESH:D009336] (4019)   Osteonecrosis [MESH:D010020] (537)   Femur Head Necrosis [MESH:D005271] (266)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  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)   Shock, Hemorrhagic [MESH:D012771] (2042)  Signs and Symptoms [MESH:D012816] (10659)   Aging, Premature [MESH:D019588] (66)  Edema [MESH:D004487] (3726)  Fatigue [MESH:D005221] (437)  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)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Dyskinesias [MESH:D020820] (3285)   Ataxia [MESH:D001259] (984)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Psychomotor Agitation [MESH:D011595] (210)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)   Amnesia, Retrograde [MESH:D000648] (53)  Intellectual Disability [MESH:D008607] (1476)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Psychomotor Disorders [MESH:D011596] (576)   Psychomotor Agitation [MESH:D011595] (167)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Cramp [MESH:D009120] (135)   Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps [MESH:C567088] (77)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Hemiplegia [MESH:D006429] (184)   Familial porencephaly [MESH:C536850] (77)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Hearing Loss, Sudden [MESH:D003639] (56)  Deafness [MESH:D003638] (593)   Mental retardation-hypotonic facies syndrome, x-linked, 1 [MESH:C537457] (59)  Hearing Loss, Conductive [MESH:D006314] (134)   Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness [MESH:C565046] (89)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Chudley-Mccullough syndrome [MESH:C535459] (45)  Marshall syndrome [MESH:C536025] (52)  Stickler syndrome, type 1 [MESH:C537492] (89)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperoxia [MESH:D018496] (694)  Hyperventilation [MESH:D006985] (652)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Skin Manifestations [MESH:D012877] (1250)   Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Urological Manifestations [MESH:D020924] (3532)   Lower Urinary Tract Symptoms [MESH:D059411] (612)   Urinary Bladder, Overactive [MESH:D053201] (530)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Mercury Poisoning [MESH:D008630] (193)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   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)  Fractures, Bone [MESH:D050723] (597)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Alcohols [MESH:D000438] (4074)   Glycols [MESH:D006018] (1181)   Ethylene Glycols [MESH:D005026] (768) 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)   Facies [MESH:D019066] (704)   Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Macrocephaly Autism Syndrome [MESH:C565342] (151) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Mental Disorders [MESH:D001523] (2063)   Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Dementia [MESH:D003704] (471)   Alzheimer Disease [MESH:D000544] (242)   Alzheimer disease type 2 [MESH:C536595] (165)  Lewy Body Disease [MESH:D020961] (139)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Child Development Disorders, Pervasive [MESH:D002659] (157)   Autistic Disorder [MESH:D001321] (154)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Intellectual Disability [MESH:D008607] (1109)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mowat-Wilson syndrome [MESH:C536990] (37)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Cerebral Cavernous Malformations 2 [MESH:C566394] (13)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XY Disorders of Sex Development [MESH:D058490] (388)   Lipoid congenital adrenal hyperplasia [MESH:C537027] (289)