Item 6 of 72 (back to results) previous next   triadimefon C032910               MeSH Unique Identifier: C032910 Chemical – Gene Interaction Note 1: Triadimefon results in increased expression of ABCB1 mRNA Note 2: Triadimefon inhibits the reaction [Metribolone results in increased activity of AR protein] Click here for more information

Current search: C15. Hemic and Lymphatic Diseases: Hematologic Diseases [MESH:D006402] > Blood Group Incompatibility [MESH:D001787] × C20. Immune System Diseases: Z. Exceptions × 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 B [HGNC:ABCB] (452)   ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355)  CD molecules [HGNC:CD] (1459)   ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 19, subfamily A, polypeptide 01 [HGNC:CYP19A1] (210)  EPH receptors [HGNC:EPH] (55)   EPH receptor A2 [HGNC:EPHA2] (24)  Fibronectin type III domain containing [HGNC:FN3] (399)   EPH receptor A2 [HGNC:EPHA2] (24)  Nuclear hormone receptors [HGNC:NR] (1322)   estrogen receptor 1 [HGNC:ESR1] (506)  nuclear receptor subfamily 1, group I, member 2 [HGNC:NR1I2] (328)  Sterile alpha motif (SAM) containing [HGNC:SAMD] (92)   EPH receptor A2 [HGNC:EPHA2] (24) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  Decreases (5154)   activity (2549)  expression (2187)  reaction (3393)  Increases (5571)   activity (2865)  expression (3238) 4. Semantic Terms  4. Semantic Terms  Entity [STY:T071] (48056)   Physical Object [STY:T072] (47583)   Substance [STY:T167] (46174)   Chemical [STY:T103] (46110)   Chemical Viewed Functionally [STY:T120] (28747)   Pharmacologic Substance [STY:T121] (11019)  Chemical Viewed Structurally [STY:T104] (44741)   Organic Chemical [STY:T109] (44144) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Head [MESH:D006257] (523)   Ear [MESH:D004423] (236)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Face [MESH:D005145] (387)   Mouth [MESH:D009055] (40)   Lip [MESH:D008046] (39)   Van der Woude syndrome [MESH:C536528] (33)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Joints [MESH:D007596] (126)   Knee Joint [MESH:D007719] (38)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Nervous System [MESH:D009420] (587)   Central Nervous System [MESH:D002490] (371)   Brain [MESH:D001921] (349)   Brain Stem [MESH:D001933] (120)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Stomatognathic System [MESH:D013284] (673)   Mouth [MESH:D009055] (194)   Dentition [MESH:D003817] (109)   Tooth [MESH:D014070] (61)   Incisor [MESH:D007180] (51)   Single upper central incisor [MESH:C537342] (50)  Lip [MESH:D008046] (42)   Van der Woude syndrome [MESH:C536528] (33) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Pasteurellaceae Infections [MESH:D016871] (348)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Skin Diseases, Bacterial [MESH:D017192] (157)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)  Eye Infections [MESH:D015817] (86)   Corneal Ulcer [MESH:D003320] (61)  Skin Diseases, Infectious [MESH:D012874] (415)   Skin Diseases, Bacterial [MESH:D017192] (156)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Suppuration [MESH:D013492] (219)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Visceral [MESH:D007898] (2149)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Hamartoma [MESH:D006222] (1484)  Neoplasms, Second Primary [MESH:D016609] (518)  Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Van der Woude syndrome [MESH:C536528] (33)  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, Myeloid, Acute [MESH:D015470] (2176)  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)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Osteosarcoma [MESH:D012516] (2175)  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)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Adenoma, Liver Cell [MESH:D018248] (685)  Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Keratoacanthoma familial [MESH:C536150] (78)  Carcinoma, Lewis Lung [MESH:D018827] (248)  Carcinoma, Small Cell [MESH:D018288] (1317)  Adenocarcinoma [MESH:D000230] (6565)   Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  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, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   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)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Meningioma [MESH:D008579] (978)  Neoplasms by Site [MESH:D009371] (9169)   Skin Neoplasms [MESH:D012878] (2992)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Digestive System Neoplasms [MESH:D004067] (7487)   Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)   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)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Head and Neck Neoplasms [MESH:D006258] (4612)   Thyroid Neoplasms [MESH:D013964] (2040)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  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)   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, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Carcinoma, Lewis Lung [MESH:D018827] (248)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Resorption [MESH:D001862] (2352)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromicric dysplasia [MESH:C535662] (520)  Dwarfism [MESH:D004392] (778)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Syndactyly [MESH:D013576] (487)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Osteochondrodysplasias [MESH:D010009] (2440)   Spondylo-Megaepiphyseal-Metaphyseal Dysplasia [MESH:C567639] (11)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Bone Diseases, Endocrine [MESH:D001849] (747)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  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)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Joint Diseases [MESH:D007592] (4657)   Arthralgia [MESH:D018771] (191)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Muscular Diseases [MESH:D009135] (4071)   Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Myositis [MESH:D009220] (2071)   Polymyositis [MESH:D017285] (2007)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Syndactyly [MESH:D013576] (487)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Syndactyly [MESH:D013576] (487)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  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)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Cholestasis, progressive familial intrahepatic 3 [MESH:C535935] (101)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Cholangitis [MESH:D002761] (203)   Cholangitis, Sclerosing [MESH:D015209] (93)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Cholelithiasis [MESH:D002769] (373)   Gallstones [MESH:D042882] (350)  Gallbladder Diseases [MESH:D005705] (1215)   Cholecystolithiasis [MESH:D041761] (353)   Gallstones [MESH:D042882] (350)  Digestive System Neoplasms [MESH:D004067] (7493)   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)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  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)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  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)  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)   Sitosterolemia [MESH:C537345] (82)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)  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)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  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 Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Liver Diseases [MESH:D008107] (8167)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatomegaly [MESH:D006529] (1169)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Cholestasis, progressive familial intrahepatic 3 [MESH:C535935] (101)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   End Stage Liver Disease [MESH:D058625] (108)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Animal [MESH:D006520] (260)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Peritoneal Diseases [MESH:D010532] (1119)   Peritoneal Fibrosis [MESH:D056627] (488) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Mouth Diseases [MESH:D009059] (4783)   Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Periodontal Diseases [MESH:D010510] (1001)   Periodontitis [MESH:D010518] (843)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Respiratory System Abnormalities [MESH:D015619] (243)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchiectasis [MESH:D001987] (1792)  Lung Diseases [MESH:D008171] (7249)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Cystic Fibrosis [MESH:D003550] (760)  Pneumonia [MESH:D011014] (3482)  Pulmonary Fibrosis [MESH:D011658] (3140)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Neoplasms [MESH:D008175] (6012)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   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)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  Retrocochlear Diseases [MESH:D012181] (241)   Auditory Diseases, Central [MESH:D001304] (210)   Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)   Hypotension, Orthostatic [MESH:D007024] (679)  Central Nervous System Diseases [MESH:D002493] (9745)   Meningitis [MESH:D008581] (352)  Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Auditory Diseases, Central [MESH:D001304] (210)   Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Kernicterus [MESH:D007647] (256)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Peroxisomal Disorders [MESH:D018901] (1472)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Cerebrovascular Disorders [MESH:D002561] (5542)   Stroke [MESH:D020521] (3702)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  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)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)   Frontotemporal Dementia [MESH:D057180] (300)   Pick Disease of the Brain [MESH:D020774] (184)  Epilepsy [MESH:D004827] (6274)   Status Epilepticus [MESH:D013226] (4014)  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)   Hypopituitarism [MESH:D007018] (732)  Central Nervous System Infections [MESH:D002494] (1823)   Meningitis [MESH:D008581] (1506)  Movement Disorders [MESH:D009069] (4823)   Dystonic Disorders [MESH:D020821] (729)   Juvenile-onset dystonia [MESH:C537704] (143)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Ocular Motility Disorders [MESH:D015835] (364)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Nervous System Malformations [MESH:D009421] (3354)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Malformations of Cortical Development [MESH:D054220] (1406)   Neuronal Migration Disorders [MESH:D054081] (264)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   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)   Rett Syndrome [MESH:D015518] (143)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Paralysis [MESH:D010243] (2043)  Dyskinesias [MESH:D020820] (3365)   Dystonia [MESH:D004421] (848)  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)   Mental Retardation, X-Linked [MESH:D038901] (1854)   Fragile X Syndrome [MESH:D005600] (353)  Rett Syndrome [MESH:D015518] (143)  Psychomotor Disorders [MESH:D011596] (576)   Apraxias [MESH:D001072] (118)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Pain [MESH:D010146] (3875)   Neuralgia [MESH:D009437] (2074)  Paresis [MESH:D010291] (419)   Paraparesis [MESH:D020335] (77)   Paraparesis, Spastic [MESH:D020336] (70)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  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 Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Muscular Diseases [MESH:D009135] (3538)   Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Myositis [MESH:D009220] (2069)   Polymyositis [MESH:D017285] (2007)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  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)   Keratitis [MESH:D007634] (168)   Corneal Ulcer [MESH:D003320] (61)  Eye Abnormalities [MESH:D005124] (1233)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Coloboma [MESH:D003103] (315)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Albinism [MESH:D000417] (258)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Eye Infections [MESH:D015817] (110)   Corneal Ulcer [MESH:D003320] (61)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)  Ocular Motility Disorders [MESH:D015835] (1699)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157) 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)   Aromatase deficiency [MESH:C537436] (277)  Asthenozoospermia [MESH:D053627] (298)  Oligospermia [MESH:D009845] (799)  Penile Diseases [MESH:D010409] (1805)   Penile Induration [MESH:D010411] (495)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Urogenital Abnormalities [MESH:D014564] (2065)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Urogenital Abnormalities [MESH:D014564] (2043)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (5792)   Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)  Pregnancy Complications [MESH:D011248] (4768)   Intrahepatic Cholestasis of Pregnancy [MESH:C535932] (101)  Hyperthyroidism, Familial Gestational [MESH:C566384] (39)  Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Prenatal Injuries [MESH:D049188] (1314) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Heterotaxy Syndrome [MESH:D059446] (84)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)  Cardiomyopathy, Dilated, 1u [MESH:C566296] (56)  Cardiomyopathies [MESH:D009202] (5331)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)  Cardiomyopathy, Dilated, 1u [MESH:C566296] (56)  Heart Defects, Congenital [MESH:D006330] (2443)   Heterotaxy Syndrome [MESH:D059446] (84)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  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)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Vascular Diseases [MESH:D014652] (8691)   Arteritis [MESH:D001167] (1084)  Hypertension [MESH:D006973] (5655)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Cerebrovascular Disorders [MESH:D002561] (5541)   Stroke [MESH:D020521] (3702)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  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)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Thrombosis [MESH:D013927] (3101)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  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)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Raynaud Disease [MESH:D011928] (490)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Adenosine Triphosphate, Elevated, Of Erythrocytes [MESH:C566310] (78)  Methemoglobinemia [MESH:D008708] (850)  Anemia [MESH:D000740] (3966)   Anemia, Hemolytic [MESH:D000743] (3083)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Blood Coagulation Disorders [MESH:D001778] (1828)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Kernicterus [MESH:D007647] (256)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Hypergammaglobulinemia [MESH:D006942] (137)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic Syndromes [MESH:D009190] (2093)  Myeloproliferative Disorders [MESH:D009196] (1492)   Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemorrhagic Disorders [MESH:D006474] (3359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Leukocyte Disorders [MESH:D007960] (2662)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphoproliferative Disorders [MESH:D008232] (4638)   Sarcoidosis [MESH:D012507] (895)  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)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Splenic Diseases [MESH:D013158] (1323)   Heterotaxy Syndrome [MESH:D059446] (84) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Drug-Induced [MESH:D000014] (1024)  Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Van der Woude syndrome [MESH:C536528] (33)  Heterotaxy Syndrome [MESH:D059446] (84)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Heterotaxy Syndrome [MESH:D059446] (84)  Chromosome Disorders [MESH:D025063] (2030)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Eye Abnormalities [MESH:D005124] (1233)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Coloboma [MESH:D003103] (315)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Lower Extremity Deformities, Congenital [MESH:D038061] (81)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Syndactyly [MESH:D013576] (487)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Syndactyly [MESH:D013576] (487)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Nervous System Malformations [MESH:D009421] (3354)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Malformations of Cortical Development [MESH:D054220] (1406)   Neuronal Migration Disorders [MESH:D054081] (264)  Neural Tube Defects [MESH:D009436] (2143)   Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Skin Abnormalities [MESH:D012868] (1723)   Ichthyosis [MESH:D007057] (481)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Cleft Palate [MESH:D002972] (1330)   Van der Woude syndrome [MESH:C536528] (33)  Popliteal Pterygium Syndrome [MESH:C562509] (33)  Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Urogenital Abnormalities [MESH:D014564] (2064)   Popliteal Pterygium Syndrome [MESH:C562509] (33)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Genetic Diseases, Inborn [MESH:D030342] (9766)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Cystic Fibrosis [MESH:D003550] (760)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Chromosome Disorders [MESH:D025063] (2030)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Dwarfism [MESH:D004392] (783)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Fragile X Syndrome [MESH:D005600] (353)  Rett Syndrome [MESH:D015518] (143)  Hereditary Autoinflammatory Diseases [MESH:D056660] (272)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Rett Syndrome [MESH:D015518] (143)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Fragile X Syndrome [MESH:D005600] (353)  Rett Syndrome [MESH:D015518] (143)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Aromatase deficiency [MESH:C537436] (277)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  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)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Peroxisomal Disorders [MESH:D018901] (1472)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Gilbert Disease [MESH:D005878] (259)  Crigler-Najjar Syndrome [MESH:D003414] (255)   Crigler Najjar syndrome, type 2 [MESH:C536213] (254)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Sitosterolemia [MESH:C537345] (82)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Peroxisomal Disorders [MESH:D018901] (1788)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Skin Diseases, Genetic [MESH:D012873] (3456)   Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Porokeratosis [MESH:D017499] (59)   Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Cystic Fibrosis [MESH:D003550] (760)  Erythroblastosis, Fetal [MESH:D004899] (257)   Kernicterus [MESH:D007647] (256)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Ichthyosis [MESH:D007057] (476)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Penile Induration [MESH:D010411] (495)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Panniculitis [MESH:D015434] (91)   Panniculitis, Nodular Nonsuppurative [MESH:D010201] (78)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Exanthema [MESH:D005076] (301)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Gynecomastia [MESH:D006177] (484)   Aromatase deficiency [MESH:C537436] (277)  Dermatitis [MESH:D003872] (4530)   Drug Eruptions [MESH:D003875] (2697)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136)  Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Keratoacanthoma [MESH:D007636] (83)   Keratoacanthoma familial [MESH:C536150] (78)  Keratosis [MESH:D007642] (1941)   Ichthyosis [MESH:D007057] (481)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Porokeratosis [MESH:D017499] (59)   Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52)  Panniculitis [MESH:D015434] (88)   Panniculitis, Nodular Nonsuppurative [MESH:D010201] (78)  Pigmentation Disorders [MESH:D010859] (1215)   Hypopigmentation [MESH:D017496] (718)   Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Skin Abnormalities [MESH:D012868] (1709)   Ichthyosis [MESH:D007057] (481)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Albinism [MESH:D000417] (359)   Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Porokeratosis [MESH:D017499] (59)   Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Bacterial [MESH:D017192] (156)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Urticaria [MESH:D014581] (2668)  Sweat Gland Diseases [MESH:D013543] (231)   Hidradenitis [MESH:D016575] (121)   Hidradenitis Suppurativa [MESH:D017497] (120)   Hidradenitis suppurativa, familial [MESH:C538118] (67) 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)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Kernicterus [MESH:D007647] (256)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Peroxisomal Disorders [MESH:D018901] (1472)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Hypercalcemia [MESH:D006934] (1999)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  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)  Xanthomatosis [MESH:D014973] (145)  Dyslipidemias [MESH:D050171] (2428)   Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Hyperlipidemias [MESH:D006949] (1908)   Hypertriglyceridemia [MESH:D015228] (808)  Hypercholesterolemia [MESH:D006937] (1404)   Sitosterolemia [MESH:C537345] (82)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Sitosterolemia [MESH:C537345] (82)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Aromatase deficiency [MESH:C537436] (277)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  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)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Peroxisomal Disorders [MESH:D018901] (1472)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Gilbert Disease [MESH:D005878] (259)  Crigler-Najjar Syndrome [MESH:D003414] (255)   Crigler Najjar syndrome, type 2 [MESH:C536213] (254)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Sitosterolemia [MESH:C537345] (82)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Peroxisomal Disorders [MESH:D018901] (1788)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Smith-Lemli-Opitz Syndrome [MESH:D019082] (100)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Mitochondrial Diseases [MESH:D028361] (2561)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   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)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Porphyria, Variegate [MESH:D046350] (50)   Porphyria, South African type [MESH:C538659] (48)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Thiamine Deficiency [MESH:D013832] (139)  Vitamin D Deficiency [MESH:D014808] (360)   Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Vitamin D Hydroxylation-Deficient Rickets, Type 1A [MESH:C562688] (58)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Obesity, Abdominal [MESH:D056128] (115) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Adrenal Cortex Diseases [MESH:D000303] (969)   Pigmented Nodular Adrenocortical Disease, Primary, 2 [MESH:C566472] (21)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Dwarfism [MESH:D004392] (698)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Delayed [MESH:D011628] (449)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Gonadal Dysgenesis [MESH:D006059] (492)   Sexual Infantilism [MESH:D050035] (277)  Hypogonadism [MESH:D007006] (1123)   Sexual Infantilism [MESH:D050035] (277)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Pituitary Diseases [MESH:D010900] (1829)   Hypopituitarism [MESH:D007018] (732)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040)  Thyrotoxicosis [MESH:D013971] (93)  Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)  Hyperthyroidism [MESH:D006980] (1191)   Hyperthyroidism, Nonautoimmune [MESH:C563786] (39)  Thyroid Hormone Resistance, Selective Pituitary [MESH:C564154] (113)  Hyperthyroidism, Familial Gestational [MESH:C566384] (39)  Graves Disease [MESH:D006111] (278)  Thyrotoxicosis [MESH:D013971] (93)  Hyperthyroxinemia [MESH:D006981] (659)   Thyroid Hormone Resistance Syndrome [MESH:D018382] (135)   Thyroid Hormone Resistance, Generalized, Autosomal Dominant [MESH:C567934] (113)  Thyroid Hormone Resistance, Generalized, Autosomal Recessive [MESH:C567936] (113)  Hypothyroidism [MESH:D007037] (496)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Thyroiditis [MESH:D013966] (158)   Thyroiditis, Autoimmune [MESH:D013967] (149) C20. Immune System Diseases  C20. Immune System Diseases  Z. Exceptions (350)   Not Fully Specified [NFS] (350)  Immune System Diseases [MESH:D007154] (7674)   Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Graves Disease [MESH:D006111] (278)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Thyroiditis, Autoimmune [MESH:D013967] (79)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Kernicterus [MESH:D007647] (256)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Urticaria [MESH:D014581] (2668)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)  Immunoproliferative Disorders [MESH:D007160] (4761)   Hypergammaglobulinemia [MESH:D006942] (137)   Mevalonate Kinase Deficiency [MESH:D054078] (38)  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)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Hepatitis, Animal [MESH:D006520] (260)  Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Atrophy [MESH:D001284] (2603)  Plaque, Amyloid [MESH:D058225] (334)  Ventricular Remodeling [MESH:D020257] (686)  Alopecia [MESH:D000505] (1383)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Calculi [MESH:D002137] (756)   Gallstones [MESH:D042882] (350)  Cysts [MESH:D003560] (133)   Van der Woude syndrome [MESH:C536528] (33)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  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)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Translocation, Genetic [MESH:D014178] (557)  Disease Attributes [MESH:D020969] (3654)   Critical Illness [MESH:D016638] (296)  Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)  Recurrence [MESH:D012008] (830)  Emphysema [MESH:D004646] (1096)   Subcutaneous Emphysema [MESH:D013352] (82)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Fibrosis [MESH:D005355] (3133)   Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Hemorrhage [MESH:D006470] (4451)   Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Hyperbilirubinemia [MESH:D006932] (1860)   Kernicterus [MESH:D007647] (256)  Hyperbilirubinemia, Neonatal [MESH:D051556] (258)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Pain, Postoperative [MESH:D010149] (529)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Signs and Symptoms [MESH:D012816] (10659)   Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Feminization [MESH:D005262] (655)  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)   Paralysis [MESH:D010243] (2298)  Dyskinesias [MESH:D020820] (3285)   Dystonia [MESH:D004421] (848)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Apraxias [MESH:D001072] (114)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Psychomotor Disorders [MESH:D011596] (576)   Apraxias [MESH:D001072] (118)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Pain [MESH:D010146] (3869)   Neuralgia [MESH:D009437] (2074)  Paresis [MESH:D010291] (419)   Paraparesis [MESH:D020335] (77)   Paraparesis, Spastic [MESH:D020336] (70)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Microtia, Hearing Impairment, And Cleft Palate [MESH:C567359] (30)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Athabaskan brainstem dysgenesis [MESH:C535397] (40)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  Pain [MESH:D010146] (4511)   Arthralgia [MESH:D018771] (191)  Neuralgia [MESH:D009437] (2074)  Pain, Postoperative [MESH:D010149] (529)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  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)  Skin Manifestations [MESH:D012877] (1250)   Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)  Virilism [MESH:D014770] (327)   Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136) 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)   Drug Eruptions [MESH:D003875] (2697)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Neurotoxicity Syndromes [MESH:D020258] (3323)  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)  Phencyclidine Abuse [MESH:D010623] (288)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950) C26. Wounds and Injuries  C26. Wounds and Injuries  Wounds and Injuries [MESH:D014947] (5171)   Spinal Cord Injuries [MESH:D013119] (2688)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D03. Heterocyclic Compounds  D03. Heterocyclic Compounds  Heterocyclic Compounds [MESH:D006571] (56330)   Heterocyclic Compounds, 1-Ring [MESH:D006573] (30631)   Azoles [MESH:D001393] (10398)   Triazoles [MESH:D014230] (727) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Apraxias [MESH:D001072] (83)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Psychomotor Disorders [MESH:D011596] (250)   Apraxias [MESH:D001072] (83)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Mental Disorders [MESH:D001523] (2063)   Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Dementia [MESH:D003704] (471)   Alzheimer Disease [MESH:D000544] (242)   Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia [MESH:C564330] (56)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XX Disorders of Sex Development [MESH:D058489] (375)   Cortisone reductase deficiency [MESH:C536447] (136)  Aromatase deficiency [MESH:C537436] (277)