Item 11 of 57 (back to results) previous next   BEP protocol C038328               MeSH Unique Identifier: C038328 Scope Notes: Chemotherapy protocol consisting of above cpds; used in treatment of testicular neoplasms Click here for more information

Current search: C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Urogenital Abnormalities [MESH:D014564] > Disorders of Sex Development [MESH:D012734] > 46, XY Disorders of Sex Development [MESH:D058490] > Gonadal Dysgenesis, 46,XY [MESH:D006061] > Meacham Winn Culler syndrome [MESH:C538162] × 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)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Atria [MESH:D006325] (65)   Atrial myxoma, familial [MESH:C538262] (34)  Sense Organs [MESH:D012679] (1060)   Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Uvea [MESH:D014602] (270)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Cells [MESH:D002477] (1885)   Blood Cells [MESH:D001773] (196)   Erythrocytes [MESH:D004912] (146)   Erythrocytes, Abnormal [MESH:D004913] (141)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127)  Cellular Structures [MESH:D022082] (1562)   Inclusion Bodies [MESH:D002479] (147)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127)  Hemic and Immune Systems [MESH:D006424] (272)   Blood [MESH:D001769] (200)   Blood Cells [MESH:D001773] (194)   Erythrocytes [MESH:D004912] (146)   Erythrocytes, Abnormal [MESH:D004913] (141)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127) 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) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   RNA Virus Infections [MESH:D012327] (4215)   Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphatic Vessel Tumors [MESH:D018190] (171)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Myxoma [MESH:D009232] (78)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Teratocarcinoma [MESH:D018243] (3)  Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)  Glioma [MESH:D005910] (4261)   Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Adenoma, Liver Cell [MESH:D018248] (685)  Mesothelioma [MESH:D008654] (2567)  Carcinoma [MESH:D002277] (7263)   Thyroid cancer, papillary [MESH:C536915] (111)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)  Glioma [MESH:D005910] (4261)   Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)  Glioma [MESH:D005910] (4261)   Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioblastoma [MESH:D018325] (395)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Breast Neoplasms [MESH:D001943] (6077)  Skin Neoplasms [MESH:D012878] (2992)  Abdominal Neoplasms [MESH:D000008] (74)   Retroperitoneal Neoplasms [MESH:D012186] (8)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5358)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Rectal Neoplasms [MESH:D012004] (717)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Testicular Neoplasms [MESH:D013736] (520)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Head and Neck Neoplasms [MESH:D006258] (4612)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Heart Neoplasms [MESH:D006338] (47)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Neoplastic Processes [MESH:D009385] (5317)   Anaplasia [MESH:D000708] (348)  Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Bone Diseases, Developmental [MESH:D001848] (3315)   Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  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)   Pycnodysostosis [MESH:D058631] (73)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Osteoarthritis [MESH:D010003] (1743)  Muscular Diseases [MESH:D009135] (4071)   Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Limb Deformities, Congenital [MESH:D017880] (1813)   Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  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)   Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Rectal Neoplasms [MESH:D012004] (717)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Gastroenteritis [MESH:D005759] (4066)   Colitis [MESH:D003092] (3199)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Rectal Neoplasms [MESH:D012004] (717)  Intestinal Diseases [MESH:D007410] (6206)   Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Rectal Neoplasms [MESH:D012004] (717)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Rectal Neoplasms [MESH:D012004] (717)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Liver Diseases [MESH:D008107] (8167)   Cholestasis, Intrahepatic [MESH:D002780] (1510)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Fatty Liver [MESH:D005234] (3584)  Hepatitis [MESH:D006505] (3883)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatorenal Syndrome [MESH:D006530] (910)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Stomatognathic System Abnormalities [MESH:D018640] (1705)   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)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Lung Diseases [MESH:D008171] (7249)   Hypertension, Pulmonary [MESH:D006976] (2000)  Lung Injury [MESH:D055370] (3688)  Pneumonia [MESH:D011014] (3482)  Pulmonary Embolism [MESH:D011655] (1118)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Idiopathic Interstitial Pneumonias [MESH:D054988] (314)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Pulmonary Emphysema [MESH:D011656] (1259)  Lung Neoplasms [MESH:D008175] (6012)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Pulmonary Fibrosis [MESH:D011658] (3140)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pneumonia [MESH:D011014] (3482)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Wernicke Encephalopathy [MESH:D014899] (75)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Epilepsy [MESH:D004827] (6274)   Pyridoxine-dependent epilepsy [MESH:C536254] (53)  Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1250)   Hyperprolactinemia [MESH:D006966] (603)  Leukoencephalopathies [MESH:D056784] (1916)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Central Nervous System Infections [MESH:D002494] (1823)   Prion Diseases [MESH:D017096] (488)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Guanidinoacetate methyltransferase deficiency [MESH:C537622] (60)  Dystonic Disorders [MESH:D020821] (729)  Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Spinal Cord Diseases [MESH:D013118] (4376)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Demyelinating Diseases [MESH:D003711] (2917)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurodegenerative Diseases [MESH:D019636] (6613)   Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 1 [MESH:C564953] (32)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Prion Diseases [MESH:D017096] (475)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  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)   Dystonia [MESH:D004421] (848)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)   Guanidinoacetate methyltransferase deficiency [MESH:C537622] (60)  Speech Disorders [MESH:D013064] (482)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Aphasia [MESH:D001037] (219)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Korsakoff Syndrome [MESH:D020915] (69)  Intellectual Disability [MESH:D008607] (3054)   Brunner Syndrome [MESH:C563156] (124)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Down Syndrome [MESH:D004314] (1287)  WAGR Syndrome [MESH:D017624] (270)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Siderius X-linked mental retardation syndrome [MESH:C537333] (17)  Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Paralysis [MESH:D010243] (2043)   Hemiplegia [MESH:D006429] (184)  Ophthalmoplegia [MESH:D009886] (1468)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Pupil Disorders [MESH:D011681] (194)   Pierson syndrome [MESH:C537185] (33)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  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)   Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Brachial Plexus Neuropathies [MESH:D020516] (37)   Brachial Plexus Neuritis [MESH:D020968] (31)  Neuritis [MESH:D009443] (55)   Brachial Plexus Neuritis [MESH:D020968] (31)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69)  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)   Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)   Insomnia, Fatal Familial [MESH:D034062] (98)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eye Abnormalities [MESH:D005124] (1233)   Pierson syndrome [MESH:C537185] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Graves Ophthalmopathy [MESH:D049970] (165)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Pupil Disorders [MESH:D011681] (230)   Pierson syndrome [MESH:C537185] (33)  Uveal Diseases [MESH:D014603] (2428)   Iris Diseases [MESH:D007499] (348)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270) 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)  Testicular Neoplasms [MESH:D013736] (520)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Asthenozoospermia [MESH:D053627] (298)  Oligospermia [MESH:D009845] (799)   Follicle-stimulating hormone deficiency, isolated [MESH:C537070] (185)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Urogenital Abnormalities [MESH:D014564] (2065)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Denys-Drash Syndrome [MESH:D030321] (57)  Frasier Syndrome [MESH:D052159] (57)  WAGR Syndrome [MESH:D017624] (270)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Gonadal Dysgenesis [MESH:D006059] (492)   Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)   Pierson syndrome [MESH:C537185] (33)  Mesangial sclerosis, diffuse [MESH:C537346] (33)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)   Frasier Syndrome [MESH:D052159] (57)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)   Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Uterine Diseases [MESH:D014591] (2479)   Uterine Neoplasms [MESH:D014594] (2430)  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)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Denys-Drash Syndrome [MESH:D030321] (57)  Frasier Syndrome [MESH:D052159] (57)  WAGR Syndrome [MESH:D017624] (270)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Gonadal Dysgenesis [MESH:D006059] (492)   Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)   Pierson syndrome [MESH:C537185] (33)  Mesangial sclerosis, diffuse [MESH:C537346] (33)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)   Frasier Syndrome [MESH:D052159] (57)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)   Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)   Embryo Loss [MESH:D020964] (288)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Cardiovascular Diseases [MESH:D002318] (10123)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Heart Septal Defects [MESH:D006343] (385)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)  Ventricular Fibrillation [MESH:D014693] (624)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathies [MESH:D009202] (5331)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Heart Defects, Congenital [MESH:D006330] (2443)   Heart Septal Defects [MESH:D006343] (385)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  Heart Neoplasms [MESH:D006338] (47)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Heart Rupture [MESH:D006341] (141)   Heart Rupture, Post-Infarction [MESH:D006342] (137)  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)  Angina, Unstable [MESH:D000789] (782)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Vascular Diseases [MESH:D014652] (8691)   Diabetic Angiopathies [MESH:D003925] (1984)  Hypotension [MESH:D007022] (4045)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Coronary Aneurysm [MESH:D003323] (204)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Embolism, Fat [MESH:D004620] (261)   Embolism, Cholesterol [MESH:D017700] (255)  Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Thrombosis [MESH:D013927] (3101)   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)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  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)  Angina, Unstable [MESH:D000789] (782)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Raynaud Disease [MESH:D011928] (490)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Purpura, Schoenlein-Henoch [MESH:D011695] (266) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Methemoglobinemia [MESH:D008708] (850)  Polycythemia [MESH:D011086] (412)  Anemia [MESH:D000740] (3966)   Anemia, Hemolytic [MESH:D000743] (3083)   CD59 Deficiency [MESH:C567355] (57)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Heinz Body Anemias [MESH:C563030] (127)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Anemia, Sideroblastic [MESH:D000756] (636)   X-linked sideroblastic anemia [MESH:C536761] (58)  Anemia, Hypochromic Microcytic, With Iron Overload [MESH:C567144] (85)  Blood Coagulation Disorders [MESH:D001778] (1828)   Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Sideroblastic [MESH:D000756] (636)   X-linked sideroblastic anemia [MESH:C536761] (58)  Anemia, Hypochromic Microcytic, With Iron Overload [MESH:C567144] (85)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Polycythemia Vera [MESH:D011087] (244)  Hemoglobinopathies [MESH:D006453] (1863)   Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)  Hemorrhagic Disorders [MESH:D006474] (3359)   Hemostatic Disorders [MESH:D020141] (2932)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphoproliferative Disorders [MESH:D008232] (4638)   Sarcoidosis [MESH:D012507] (895)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Multiple [MESH:D000015] (3192)   Pierson syndrome [MESH:C537185] (33)  Desmosterolosis [MESH:C566555] (85)  Carney Complex [MESH:D056733] (45)  Down Syndrome [MESH:D004314] (1287)  Ectodermal Dysplasia [MESH:D004476] (938)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Heart Septal Defects [MESH:D006343] (385)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  WAGR Syndrome [MESH:D017624] (270)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Eye Abnormalities [MESH:D005124] (1233)   Pierson syndrome [MESH:C537185] (33)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Limb Deformities, Congenital [MESH:D017880] (1813)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  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)  Skin Abnormalities [MESH:D012868] (1723)   Carney Complex [MESH:D056733] (45)  Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Urogenital Abnormalities [MESH:D014564] (2064)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Denys-Drash Syndrome [MESH:D030321] (57)  Frasier Syndrome [MESH:D052159] (57)  WAGR Syndrome [MESH:D017624] (270)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Gonadal Dysgenesis [MESH:D006059] (492)   Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Frasier Syndrome [MESH:D052159] (57)  Pycnodysostosis [MESH:D058631] (73)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Heinz Body Anemias [MESH:C563030] (127)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  WAGR Syndrome [MESH:D017624] (270)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   X-linked sideroblastic anemia [MESH:C536761] (58)  Brunner Syndrome [MESH:C563156] (124)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Siderius X-linked mental retardation syndrome [MESH:C537333] (17)  Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Hemoglobinopathies [MESH:D006453] (1863)   Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Siderius X-linked mental retardation syndrome [MESH:C537333] (17)  Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 1 [MESH:C564953] (32)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Maple Syrup Urine Disease [MESH:D008375] (127)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Desmosterolosis [MESH:C566555] (85)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 1 [MESH:C564953] (32)  Lysosomal Storage Diseases [MESH:D016464] (761)   Pycnodysostosis [MESH:D058631] (73)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Skin Diseases, Genetic [MESH:D012873] (3456)   Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Scleroderma, Systemic [MESH:D012595] (199)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Skin Diseases [MESH:D012871] (8774)   Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Scleroderma, Systemic [MESH:D012595] (199)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Occupational [MESH:D009783] (311)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)  Skin Abnormalities [MESH:D012868] (1709)   Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Occupational [MESH:D009783] (311)  Skin Diseases, Genetic [MESH:D012873] (3481)   Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Urticaria [MESH:D014581] (2668)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Brain Diseases, Metabolic [MESH:D001928] (3350)   Wernicke Encephalopathy [MESH:D014899] (75)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)  Hypoglycemia [MESH:D007003] (2420)   3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Iron Metabolism Disorders [MESH:D019189] (2139)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Desmosterolosis [MESH:C566555] (85)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 1 [MESH:C564953] (32)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Maple Syrup Urine Disease [MESH:D008375] (127)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Desmosterolosis [MESH:C566555] (85)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 1 [MESH:C564953] (32)  Lysosomal Storage Diseases [MESH:D016464] (761)   Pycnodysostosis [MESH:D058631] (73)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Mitochondrial Diseases [MESH:D028361] (2561)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Thiamine Deficiency [MESH:D013832] (139)   Wernicke Encephalopathy [MESH:D014899] (75)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)   Pigmented Nodular Adrenocortical Disease, Primary, 1 [MESH:C566469] (34)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Hyperaldosteronism [MESH:D006929] (419)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Angiopathies [MESH:D003925] (1984)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Testicular Neoplasms [MESH:D013736] (520)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Gonadal Disorders [MESH:D006058] (5088)   Hypogonadism [MESH:D007006] (1123)  Puberty, Delayed [MESH:D011628] (449)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Denys-Drash Syndrome [MESH:D030321] (57)  Frasier Syndrome [MESH:D052159] (57)  WAGR Syndrome [MESH:D017624] (270)  Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Gonadal Dysgenesis [MESH:D006059] (492)   Gonadal Dysgenesis, 46,XY [MESH:D006061] (131)   Meacham Winn Culler syndrome [MESH:C538162] (57)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Testicular Neoplasms [MESH:D013736] (520)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1259)   Hyperprolactinemia [MESH:D006966] (603)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Glomerulonephritis, IGA [MESH:D005922] (897)  Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Urticaria [MESH:D014581] (2668)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immune Complex Diseases [MESH:D007105] (782)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Plaque, Amyloid [MESH:D058225] (334)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Growth Disorders [MESH:D006130] (2438)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)  Ventricular Fibrillation [MESH:D014693] (624)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Death [MESH:D003643] (1328)   Embryo Loss [MESH:D020964] (288)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Fibrosis [MESH:D005355] (3133)   Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Hemorrhage [MESH:D006470] (4451)   Hematuria [MESH:D006417] (477)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Neoplastic Processes [MESH:D009385] (5317)   Anaplasia [MESH:D000708] (348)  Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Postoperative Complications [MESH:D011183] (5311)   Graft Occlusion, Vascular [MESH:D006083] (139)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Sclerosis [MESH:D012598] (224)   Mesangial sclerosis, diffuse [MESH:C537346] (33)  Signs and Symptoms [MESH:D012816] (10659)   Flushing [MESH:D005483] (506)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Dyskinesias [MESH:D020820] (3285)   Dystonia [MESH:D004421] (848)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)   Guanidinoacetate methyltransferase deficiency [MESH:C537622] (60)  Speech Disorders [MESH:D013064] (482)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Aphasia [MESH:D001037] (219)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Korsakoff Syndrome [MESH:D020915] (69)  Intellectual Disability [MESH:D008607] (1476)   Brunner Syndrome [MESH:C563156] (124)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Hemiplegia [MESH:D006429] (184)  Ophthalmoplegia [MESH:D009886] (1468)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Pupil Disorders [MESH:D011681] (194)   Pierson syndrome [MESH:C537185] (33)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)  Pain [MESH:D010146] (4511)   Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Respiratory Sounds [MESH:D012135] (713)  Skin Manifestations [MESH:D012877] (1250)   Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)   Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Dermatitis, Occupational [MESH:D009783] (311) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug Hypersensitivity [MESH:D004342] (4001)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Wernicke Encephalopathy [MESH:D014899] (75)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D01. Inorganic Chemicals  D01. Inorganic Chemicals  Chlorine Compounds [MESH:D017606] (460)   Cisplatin [MESH:D002945] (294)  Nitrogen Compounds [MESH:D017672] (1758)   Cisplatin [MESH:D002945] (294)  Platinum Compounds [MESH:D017671] (315)   Cisplatin [MESH:D002945] (294) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Aromatic [MESH:D006841] (19108)   Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (8627)   Naphthalenes [MESH:D009281] (3103)   Tetrahydronaphthalenes [MESH:D013764] (651)   Podophyllotoxin [MESH:D011034] (356)   Etoposide [MESH:D005047] (304) D04. Polycyclic Compounds  D04. Polycyclic Compounds  Polycyclic Compounds [MESH:D011083] (22048)   Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (9200)   Naphthalenes [MESH:D009281] (3156)   Tetrahydronaphthalenes [MESH:D013764] (651)   Podophyllotoxin [MESH:D011034] (356)   Etoposide [MESH:D005047] (304) D09. Carbohydrates  D09. Carbohydrates  Carbohydrates [MESH:D002241] (15391)   Glycoconjugates [MESH:D006001] (1937)   Glycopeptides [MESH:D006020] (439)   Bleomycin [MESH:D001761] (254)  Glycosides [MESH:D006027] (7228)   Glucosides [MESH:D005960] (1868)   Etoposide [MESH:D005047] (304) D12. Amino Acids, Peptides, and Proteins  D12. Amino Acids, Peptides, and Proteins  Peptides [MESH:D010455] (20561)   Glycopeptides [MESH:D006020] (542)   Bleomycin [MESH:D001761] (254) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Therapeutics [MESH:D013812] (1838)   Clinical Protocols [MESH:D002985] (1217)   Antineoplastic Protocols [MESH:D024221] (1216)   Antineoplastic Combined Chemotherapy Protocols [MESH:D000971] (1215)   BEP protocol [MESH:C038328] (1)  Drug Therapy [MESH:D004358] (1345)   Antineoplastic Protocols [MESH:D024221] (1216)   Antineoplastic Combined Chemotherapy Protocols [MESH:D000971] (1215)   BEP protocol [MESH:C038328] (1)  Drug Therapy, Combination [MESH:D004359] (1217)   Antineoplastic Combined Chemotherapy Protocols [MESH:D000971] (1215)   BEP protocol [MESH:C038328] (1) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Behavior [MESH:D001519] (335)   Behavioral Symptoms [MESH:D001526] (173)   Aggression [MESH:D000374] (127)   Brunner Syndrome [MESH:C563156] (124)  Social Behavior [MESH:D012919] (163)   Aggression [MESH:D000374] (125)   Brunner Syndrome [MESH:C563156] (124)  Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Brunner Syndrome [MESH:C563156] (124)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Mental Disorders [MESH:D001523] (2063)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Cognition Disorders [MESH:D003072] (115)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dementia [MESH:D003704] (471)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Impulse Control Disorders [MESH:D007174] (128)   Brunner Syndrome [MESH:C563156] (124)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Developmental Disabilities [MESH:D002658] (151)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Intellectual Disability [MESH:D008607] (1109)   Brunner Syndrome [MESH:C563156] (124)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XY Disorders of Sex Development [MESH:D058490] (388)   Persistent Mullerian duct syndrome [MESH:C536665] (47)