Item 12 of 57 (back to results) previous next   demethoxycurcumin C050229               MeSH Unique Identifier: C050229 Scope Notes: Corresponds to curcumin with one methoxy group replaced by hydrogen; isolated from rhizomes of Curcuma longa Chemical – Gene Interaction Note 1: Demethoxycurcumin results in decreased activity of ABCC1 protein Note 2: Demethoxycurcumin results in decreased activity of ABCC2 protein 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 1. Human Genes  1. Human Genes  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily C [HGNC:ABCC] (458)   ATP-binding cassette, sub-family C (CFTR/MRP), member 1 [HGNC:ABCC1] (177)  ATP-binding cassette, sub-family C (CFTR/MRP), member 2 [HGNC:ABCC2] (152)  CD molecules [HGNC:CD] (1459)   kinase insert domain receptor (a type III receptor tyrosine kinase) [HGNC:KDR] (51)  Immunoglobulin superfamily domain containing [HGNC:IGSF] (761)   V-set domain containing [HGNC:VSET] (188)   kinase insert domain receptor (a type III receptor tyrosine kinase) [HGNC:KDR] (51)  I-set domain containing [HGNC:ISET] (447)   kinase insert domain receptor (a type III receptor tyrosine kinase) [HGNC:KDR] (51)  Immunoglobulin-like domain containing [HGNC:IGD] (645)   kinase insert domain receptor (a type III receptor tyrosine kinase) [HGNC:KDR] (51)  Nuclear hormone receptors [HGNC:NR] (1322)   peroxisome proliferator-activated receptor gamma [HGNC:PPARG] (234)  ZINC FINGERS [HGNC:ZNF] (383)   Zinc fingers, C2H2-type [HGNC:ZNF] (349)   Wilms tumor 1 [HGNC:WT1] (27) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  expression (494)  Decreases (5154)   activity (2549)  expression (2187)  reaction (3393)  secretion (346)  Increases (5571)   activity (2865)  expression (3238)  secretion (901) A. Anatomy  A. Anatomy  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Skull [MESH:D012886] (610)   Facial Bones [MESH:D005147] (539)   Jaw [MESH:D007568] (524)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 21-22 and Y [MESH:D002904] (294)   Chromosomes, Human, Pair 22 [MESH:D002892] (250)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Stomatognathic System [MESH:D013284] (673)   Jaw [MESH:D007568] (528)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Urinary Tract Infections [MESH:D014552] (984)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   RNA Virus Infections [MESH:D012327] (4215)   Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   HIV Wasting Syndrome [MESH:D019247] (1956) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Helminthiasis [MESH:D006373] (1644)   Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  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)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Lymphoma, B-Cell [MESH:D016393] (2624)  Lymphoma, T-Cell [MESH:D016399] (1405)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   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)   Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Aggressive [MESH:D018222] (1562)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyosarcoma [MESH:D007890] (977)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Leiomyosarcoma [MESH:D007890] (977)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Carcinoma in Situ [MESH:D002278] (2111)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioma, capillary infantile [MESH:C535860] (190)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Thyroid Neoplasms [MESH:D013964] (2040)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   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)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   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)   Endometrial Neoplasms [MESH:D016889] (1987)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   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)  Neoplastic Processes [MESH:D009385] (5317)   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)   Hemangioma, capillary infantile [MESH:C535860] (190)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Precancerous Conditions [MESH:D011230] (2858)   Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Osteonecrosis [MESH:D010020] (539)  Bone Diseases, Developmental [MESH:D001848] (3315)   Marfan Syndrome [MESH:D008382] (646)  Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Osteochondrodysplasias [MESH:D010009] (2440)   Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  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)   Osteolysis [MESH:D010014] (1787)   Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  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)  Jaw Diseases [MESH:D007571] (1601)   Mandibular Diseases [MESH:D008336] (395)  Maxillary Diseases [MESH:D008439] (354)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Mitochondrial Myopathies [MESH:D017240] (2176)  Rhabdomyolysis [MESH:D012206] (465)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)  Limb Deformities, Congenital [MESH:D017880] (1813)   Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  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)   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)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Fatty Liver [MESH:D005234] (3584)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  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)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) 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)  Mouth Diseases [MESH:D009059] (4783)   Oral Submucous Fibrosis [MESH:D009914] (2432)  Mouth Neoplasms [MESH:D009062] (2263)   Leukoplakia, Oral [MESH:D007972] (921)  Tongue Neoplasms [MESH:D014062] (1518)  Periodontal Diseases [MESH:D010510] (1001)   Periodontitis [MESH:D010518] (843)  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) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Bronchiectasis [MESH:D001987] (1792)  Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Lung Diseases [MESH:D008171] (7249)   Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Idiopathic Interstitial Pneumonias [MESH:D054988] (314)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Neoplasms [MESH:D008175] (6012)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Pulmonary Fibrosis [MESH:D011658] (3140)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Respiratory Tract Infections [MESH:D012141] (3926)   Pleurisy [MESH:D010998] (2070)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  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) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   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)   Chronobiology Disorders [MESH:D021081] (970)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Brain Neoplasms [MESH:D001932] (2764)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   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)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   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)   Subarachnoid Hemorrhage [MESH:D013345] (1082)  Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  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)  Lewy Body Disease [MESH:D020961] (1143)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Hyperpituitarism [MESH:D006964] (1250)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Movement Disorders [MESH:D009069] (4823)   Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Nervous System Malformations [MESH:D009421] (3354)   Neural Tube Defects [MESH:D009436] (2143)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  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)  Paralysis [MESH:D010243] (2043)  Seizures [MESH:D012640] (4514)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   WAGR Syndrome [MESH:D017624] (270)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3875)   Neuralgia [MESH:D009437] (2074)  Sensation Disorders [MESH:D012678] (5011)   Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  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)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Eye Abnormalities [MESH:D005124] (1233)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma, Open-Angle [MESH:D005902] (1281)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Edema [MESH:D008269] (557)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  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)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Asthenozoospermia [MESH:D053627] (298)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Urogenital Abnormalities [MESH:D014564] (2065)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   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)  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)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hydronephrosis [MESH:D006869] (956)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  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)  Lupus Nephritis [MESH:D008181] (602)  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)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Uterine Diseases [MESH:D014591] (2479)   Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Urogenital Abnormalities [MESH:D014564] (2043)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   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)   Endometrial Neoplasms [MESH:D016889] (1989)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Denys-Drash Syndrome [MESH:D030321] (57)  WAGR Syndrome [MESH:D017624] (270)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hydronephrosis [MESH:D006869] (956)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  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)  Lupus Nephritis [MESH:D008181] (602)  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)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urethral Diseases [MESH:D014522] (955)   Urethral Obstruction [MESH:D014524] (937)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neck Obstruction [MESH:D001748] (924)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Placenta Diseases [MESH:D010922] (1781)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Prenatal Injuries [MESH:D049188] (1314)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435) 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)   Marfan Syndrome [MESH:D008382] (646)  Heart Diseases [MESH:D006331] (8614)   Cardiomegaly [MESH:D006332] (4081)  Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Pericardial Effusion [MESH:D010490] (1015)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Tachycardia [MESH:D013610] (3339)  Ventricular Fibrillation [MESH:D014693] (624)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Heart Defects, Congenital [MESH:D006330] (2443)   Marfan Syndrome [MESH:D008382] (646)  Heart Rupture [MESH:D006341] (141)   Heart Rupture, Post-Infarction [MESH:D006342] (137)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  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)  Vascular Diseases [MESH:D014652] (8691)   Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Retinal Vein Occlusion [MESH:D012170] (607)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Coronary Artery Disease [MESH:D003324] (2685)  Atherosclerosis [MESH:D050197] (4188)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   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)   Subarachnoid Hemorrhage [MESH:D013345] (1082)  Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  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)  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)   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)  Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  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)   Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Hemolytic [MESH:D000743] (3083)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  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)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Blood Protein Disorders [MESH:D001796] (3051)   Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemorrhagic Disorders [MESH:D006474] (3359)   Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Leukocyte Disorders [MESH:D007960] (2662)   Leukostasis [MESH:D018921] (769)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphoproliferative Disorders [MESH:D008232] (4638)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, B-Cell [MESH:D016393] (2624)  Lymphoma, T-Cell [MESH:D016399] (1204) 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)   Marfan Syndrome [MESH:D008382] (646)  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)   Marfan Syndrome [MESH:D008382] (646)  Chromosome Disorders [MESH:D025063] (2030)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  WAGR Syndrome [MESH:D017624] (270)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Eye Abnormalities [MESH:D005124] (1233)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)  Limb Deformities, Congenital [MESH:D017880] (1813)   Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Nervous System Malformations [MESH:D009421] (3354)   Neural Tube Defects [MESH:D009436] (2143)  Skin Abnormalities [MESH:D012868] (1723)   Ectodermal Dysplasia [MESH:D004476] (958)   Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)  Urogenital Abnormalities [MESH:D014564] (2064)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   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)  Marfan Syndrome [MESH:D008382] (646)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Chromosome Disorders [MESH:D025063] (2030)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  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)   Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Hyperhomocysteinemia [MESH:D020138] (1724)  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)   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)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  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)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Jaundice, Neonatal [MESH:D007567] (290)   Jaundice, Chronic Idiopathic [MESH:D007566] (287) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  Marfan Syndrome [MESH:D008382] (646)  Scleroderma, Localized [MESH:D012594] (1597)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Keratosis [MESH:D007642] (1941)  Scleroderma, Localized [MESH:D012594] (1597)  Skin Neoplasms [MESH:D012878] (2991)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Dermatitis [MESH:D003872] (4530)   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)  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, Allergic Contact [MESH:D017449] (3241)  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, 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)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Urticaria [MESH:D014581] (2668)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Z. Exceptions (817)   Not Fully Specified [NFS] (817)  Metabolic Diseases [MESH:D008659] (9025)   Metabolic Syndrome X [MESH:D024821] (2151)  Acid-Base Imbalance [MESH:D000137] (854)   Acidosis [MESH:D000138] (626)   Ketosis [MESH:D007662] (234)   Diabetic Ketoacidosis [MESH:D016883] (226)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   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)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Fanconi Anemia [MESH:D005199] (1604)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hypoglycemia [MESH:D007003] (2420)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetic Ketoacidosis [MESH:D016883] (226)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)  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)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipidoses [MESH:D008064] (1655)  Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypertriglyceridemia [MESH:D015228] (808)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Hyperhomocysteinemia [MESH:D020138] (1724)  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)   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)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Mitochondrial Diseases [MESH:D028361] (2561)   Mitochondrial Myopathies [MESH:D017240] (2176)  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)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hyperkalemia [MESH:D006947] (485)  Hypokalemia [MESH:D007008] (1041)  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 Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Ketoacidosis [MESH:D016883] (226)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)   Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   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)   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)  Pituitary Diseases [MESH:D010900] (1829)   Hyperpituitarism [MESH:D006964] (1259)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Glomerulonephritis, IGA [MESH:D005922] (897)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)   Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Asthma, Aspirin-Induced [MESH:D055963] (1055)  Drug Eruptions [MESH:D003875] (2695)   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)  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)  HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, B-Cell [MESH:D016393] (2624)  Lymphoma, T-Cell [MESH:D016399] (1382)  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) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   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)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Leukoplakia [MESH:D007971] (922)   Leukoplakia, Oral [MESH:D007972] (921)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Emphysema [MESH:D004646] (1096)  Fibrosis [MESH:D005355] (3133)  Gliosis [MESH:D005911] (1419)  Growth Disorders [MESH:D006130] (2438)  Hyperbilirubinemia [MESH:D006932] (1860)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Tachycardia [MESH:D013610] (3339)  Ventricular Fibrillation [MESH:D014693] (624)  Chromosome Aberrations [MESH:D002869] (2352)   Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Hemorrhage [MESH:D006470] (4451)   Hematuria [MESH:D006417] (477)  Shock, Hemorrhagic [MESH:D012771] (2042)  Intracranial Hemorrhages [MESH:D020300] (3241)   Subarachnoid Hemorrhage [MESH:D013345] (1081)  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)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Necrosis [MESH:D009336] (4019)   Osteonecrosis [MESH:D010020] (537)  Neoplastic Processes [MESH:D009385] (5317)   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)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Edema [MESH:D004487] (3726)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3869)   Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Sensation Disorders [MESH:D012678] (5009)   Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Pain [MESH:D010146] (4511)   Neuralgia [MESH:D009437] (2074)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Angina, Stable [MESH:D060050] (1702)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Nausea [MESH:D009325] (2300)  Skin Manifestations [MESH:D012877] (1250)   Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Urological Manifestations [MESH:D020924] (3532)   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)  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)  Lead Poisoning [MESH:D007855] (515)  Manganese Poisoning [MESH:D020149] (2214)  Neurotoxicity Syndromes [MESH:D020258] (3323)  Organophosphate Poisoning [MESH:D062025] (497)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Morphine Dependence [MESH:D009021] (855) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Acyclic [MESH:D006839] (3563)   Alkanes [MESH:D000473] (1061)   Heptanes [MESH:D006536] (157)   Diarylheptanoids [MESH:D036381] (124)   Curcumin [MESH:D003474] (58)  Hydrocarbons, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Aromatic [MESH:D006841] (19108)   Benzene Derivatives [MESH:D001555] (10684)   Phenols [MESH:D010636] (3676)   Catechols [MESH:D002396] (417)   Curcumin [MESH:D003474] (58)  Diarylheptanoids [MESH:D036381] (124)   Curcumin [MESH:D003474] (58) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Diagnostic Imaging [MESH:D003952] (623)   Ultrasonography [MESH:D014463] (482)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Diagnostic Techniques, Cardiovascular [MESH:D003935] (521)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457) G. Phenomena and Processes  G. Phenomena and Processes  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 21-22 and Y [MESH:D002904] (294)   Chromosomes, Human, Pair 22 [MESH:D002892] (250)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238)  Circulatory and Respiratory Physiological Phenomena [MESH:D002943] (614)   Cardiovascular Physiological Phenomena [MESH:D002320] (525)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)