Item 5 of 58 (back to results) previous next   sodium arsenate C009277               MeSH Unique Identifier: C009277 Chemical – Gene Interaction Note 1: ABCC1 protein results in decreased susceptibility to sodium arsenate Note 2: ABCC1 protein results in increased secretion of sodium arsenate 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] > Musculoskeletal Abnormalities [MESH:D009139] > Limb Deformities, Congenital [MESH:D017880] > Oculodigitoesophagoduodenal syndrome [MESH:C537734] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Aldo-keto reductases [HGNC:AKR] (282)   aldo-keto reductase family 1, member C1 [HGNC:AKR1C1] (148)  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)  Basic helix-loop-helix [HGNC:BHLH] (618)   inhibitor of DNA binding 1, dominant negative helix-loop-helix protein [HGNC:ID1] (63)  inhibitor of DNA binding 2, dominant negative helix-loop-helix protein [HGNC:ID2] (69)  inhibitor of DNA binding 3, dominant negative helix-loop-helix protein [HGNC:ID3] (47)  v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog [HGNC:MYCN] (29)  Cathepsins [HGNC:CTS] (135)   cathepsin H [HGNC:CTSH] (25)  EF-hand domain containing [HGNC:EFHAND] (226)   filaggrin [HGNC:FLG] (11)  Fatty acid binding protein family [HGNC:FABP] (151)   fatty acid binding protein 5 (psoriasis-associated) [HGNC:FABP5] (29)  Gap junction proteins (connexins) [HGNC:GJ] (78)   gap junction protein, alpha 1, 43kDa [HGNC:GJA1] (48)  Heat shock proteins [HGNC:HSP] (390)   Heat shock proteins, HSPC (HSP90) [HGNC:HSP90] (119)   TNF receptor-associated protein 1 [HGNC:TRAP1] (20)  Integrins [HGNC:ITG] (284)   integrin, beta 6 [HGNC:ITGB6] (28)  Intermediate filaments [HGNC:IF] (273)   Type I. Keratins (acidic) [HGNC:] (120)   keratin 10 [HGNC:KRT10] (27)  Keratins [HGNC:KRT] (161)   keratin 10 [HGNC:KRT10] (27)  Lectins, galactoside-binding [HGNC:LGALS] (92)   lectin, galactoside-binding, soluble, 7 [HGNC:LGALS7] (11)  Mitogen-activated protein kinase cascade [HGNC:MAP#K] (854)   Mitogen-activated protein kinases [HGNC:MAPK] (797)   mitogen-activated protein kinase 08 [HGNC:MAPK8] (234)  mitogen-activated protein kinase 09 [HGNC:MAPK9] (121)  Nuclear hormone receptors [HGNC:NR] (1322)   peroxisome proliferator-activated receptor gamma [HGNC:PPARG] (234)  Serine peptidase inhibitors, Kazal type [HGNC:SPINK] (27)   serine peptidase inhibitor, Kazal type 1 [HGNC:SPINK1] (23)  Short chain dehydrogenase/reductase superfamily [HGNC:SDR] (302)   Short chain dehydrogenase/reductase superfamily, Classical fold cluster 2 [HGNC:SDRC2] (140)   hydroxysteroid (11-beta) dehydrogenase 02 [HGNC:HSD11B2] (72)  Transglutaminases [HGNC:TGM] (82)   transglutaminase 1 [HGNC:TGM1] (15) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   cotreatment (1499)  expression (494)  response to substance (623)  Decreases (5154)   activity (2549)  expression (2187)  reaction (3393)  response to substance (713)  Increases (5571)   expression (3238)  methylation (105)  phosphorylation (1060)  reduction (162)  secretion (901) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Lower Extremity [MESH:D035002] (139)   Foot [MESH:D005528] (125)   Forefoot, Human [MESH:D005545] (118)   Toes [MESH:D014034] (115)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Hip [MESH:D006615] (9)   Ischiopatellar dysplasia [MESH:C535540] (7)  Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Syndactyly, type 3 [MESH:C538154] (192)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Head [MESH:D006257] (523)   Face [MESH:D005145] (387)   Eye [MESH:D005123] (148)   Eyelids [MESH:D005143] (143)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Nose [MESH:D009666] (71)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Leg Bones [MESH:D007867] (228)   Patella [MESH:D010329] (168)   Ischiopatellar dysplasia [MESH:C535540] (7)  Pelvic Bones [MESH:D010384] (41)   Ischium [MESH:D007512] (8)   Ischiopatellar dysplasia [MESH:C535540] (7)  Bones of Upper Extremity [MESH:D001133] (240)   Arm Bones [MESH:D050280] (183)   Ulna [MESH:D014457] (96)   Ulnar-mammary syndrome [MESH:C536937] (57)  Spine [MESH:D013131] (258)   VACTERL hydrocephaly [MESH:C536521] (151)  Lumbar Vertebrae [MESH:D008159] (47)   Spondylocarpotarsal synostosis [MESH:C535780] (44)  Thoracic Vertebrae [MESH:D013904] (46)   Spondylocarpotarsal synostosis [MESH:C535780] (44)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Intestines [MESH:D007422] (271)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Lower Gastrointestinal Tract [MESH:D041741] (254)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Upper Gastrointestinal Tract [MESH:D041742] (236)   Esophagus [MESH:D004947] (200)   VACTERL hydrocephaly [MESH:C536521] (151)  Respiratory System [MESH:D012137] (321)   Lung [MESH:D008168] (71)   Pulmonary Alveoli [MESH:D011650] (59)   Alveolar capillary dysplasia [MESH:C536590] (56)  Nose [MESH:D009666] (91)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Trachea [MESH:D014132] (190)   VACTERL hydrocephaly [MESH:C536521] (151)  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   VACTERL hydrocephaly [MESH:C536521] (151)  Cardiovascular System [MESH:D002319] (1086)   Blood Vessels [MESH:D001808] (278)   Arteries [MESH:D001158] (173)   Arterial Tortuosity Syndrome [MESH:C565942] (12)  Heart [MESH:D006321] (904)   Heart Conduction System [MESH:D006329] (263)   Cardiac Conduction Defect [MESH:C562490] (16)  Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  Sense Organs [MESH:D012679] (1060)   Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Peters anomaly [MESH:C537884] (465)  Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Eyelids [MESH:D005143] (146)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Uvea [MESH:D014602] (270)   Iris [MESH:D007498] (234)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Nose [MESH:D009666] (74)   Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Helicobacter Infections [MESH:D016481] (579)  Pseudomonas Infections [MESH:D011552] (42)  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)  Staphylococcal Infections [MESH:D013203] (264)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)  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)  Intraabdominal Infections [MESH:D059413] (958)   Peritonitis [MESH:D010538] (800)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  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)  Skin Diseases, Infectious [MESH:D012874] (415)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289)  Mycoses [MESH:D009181] (385)   Candidiasis [MESH:D002177] (307)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Encephalitis [MESH:D004660] (226)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)  Herpesviridae Infections [MESH:D006566] (1944)   Cytomegalovirus Infections [MESH:D003586] (222)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Morbillivirus Infections [MESH:D018185] (87)   Measles [MESH:D008457] (83)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  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)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   HIV Wasting Syndrome [MESH:D019247] (1956)  Slow Virus Diseases [MESH:D012897] (782)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  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)   Neoplasms, Second Primary [MESH:D016609] (518)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myelomonocytic, Acute [MESH:D015479] (85)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Leukemia, Monocytic, Acute [MESH:D007948] (98)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, 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, Extranodal NK-T-Cell [MESH:D054391] (132)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Hepatoblastoma [MESH:D018197] (548)  Wilms Tumor [MESH:D009396] (553)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Neoplasms, Adipose Tissue [MESH:D018205] (677)   Lipoma [MESH:D008067] (159)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Abdominal [MESH:D018221] (56)  Fibromatosis, Aggressive [MESH:D018222] (1562)   Desmoid disease, hereditary [MESH:C535944] (58)  Histiocytoma [MESH:D051642] (272)   Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Carcinoma, Neuroendocrine [MESH:D018278] (262)   Carcinoma, Medullary [MESH:D018276] (181)  Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Uveal melanoma [MESH:C536494] (109)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  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)   Desmoid disease, hereditary [MESH:C535944] (58)  Carcinoma [MESH:D002277] (7263)   Keratoacanthoma familial [MESH:C536150] (78)  Thyroid cancer, papillary [MESH:C536915] (111)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Lewis Lung [MESH:D018827] (248)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Adenocarcinoma, Scirrhous [MESH:D002293] (29)   Linitis Plastica [MESH:D008039] (28)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma, Neuroendocrine [MESH:D018278] (262)   Carcinoma, Medullary [MESH:D018276] (181)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Pilomatrixoma [MESH:D018296] (252)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Medullary [MESH:D018276] (181)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Carcinoma, Neuroendocrine [MESH:D018278] (184)   Carcinoma, Medullary [MESH:D018276] (181)  Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Uveal melanoma [MESH:C536494] (109)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioma, capillary infantile [MESH:C535860] (190)  Hemangioblastoma [MESH:D018325] (395)  Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Uveal melanoma [MESH:C536494] (109)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Nevus [MESH:D009506] (340)   Nevus, Pigmented [MESH:D009508] (123)   Nevus, Epidermal [MESH:C562736] (112)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Abdominal Neoplasms [MESH:D000008] (74)   Desmoid disease, hereditary [MESH:C535944] (58)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  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)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  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)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroid cancer, papillary [MESH:C536915] (111)  Eye Neoplasms [MESH:D005134] (400)   Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroid cancer, papillary [MESH:C536915] (111)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Skin Neoplasms [MESH:D012878] (2992)   Nevus, Epidermal [MESH:C562736] (112)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  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)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Neoplasms, Experimental [MESH:D009374] (5218)   Carcinoma, Lewis Lung [MESH:D018827] (248)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Neoplastic Processes [MESH:D009385] (5317)   Anaplasia [MESH:D000708] (348)  Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm 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)   Hemangioma, capillary infantile [MESH:C535860] (190)  Turcot syndrome [MESH:C536928] (159)  Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Wilms Tumor [MESH:D009396] (553)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Precancerous Conditions [MESH:D011230] (2858)   Aberrant Crypt Foci [MESH:D058739] (326)  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)   Spondylocarpotarsal synostosis [MESH:C535780] (44)  Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Osteitis Deformans [MESH:D010001] (287)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Bone Diseases, Developmental [MESH:D001848] (3315)   Ischiopatellar dysplasia [MESH:C535540] (7)  Acromicric dysplasia [MESH:C535662] (520)  Proteus Syndrome [MESH:D016715] (152)  Dwarfism [MESH:D004392] (778)   Boomerang dysplasia [MESH:C536573] (44)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12)  Cockayne Syndrome [MESH:D003057] (107)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1A [MESH:C536015] (16)  Congenital Hypothyroidism [MESH:D003409] (266)   Weaver syndrome [MESH:C536687] (16)  Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Synostosis [MESH:D013580] (817)   Spondylocarpotarsal synostosis [MESH:C535780] (44)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Osteochondrodysplasias [MESH:D010009] (2440)   Atelosteogenesis, type 1 [MESH:C535396] (44)  Cantu syndrome [MESH:C535572] (42)  Osteoglophonic dwarfism [MESH:C536050] (90)  Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Boomerang dysplasia [MESH:C536573] (44)  Stuve-Wiedemann syndrome [MESH:C537502] (66)  Omodysplasia type 1 [MESH:C537746] (13)  Larsen syndrome, dominant type [MESH:C537873] (44)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Fibrous Dysplasia of Bone [MESH:D005357] (737)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Langer-Giedion Syndrome [MESH:D015826] (25)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1A [MESH:C536015] (16)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Bruck syndrome 2 [MESH:C537407] (64)  Bone Diseases, Endocrine [MESH:D001849] (747)   Acromegaly [MESH:D000172] (466)  Congenital Hypothyroidism [MESH:D003409] (266)   Weaver syndrome [MESH:C536687] (16)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)  Hyperostosis [MESH:D015576] (493)   Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Exostoses [MESH:D005096] (160)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  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)  Spinal Curvatures [MESH:D013121] (742)   Scoliosis [MESH:D012600] (194)   Spondylocarpotarsal synostosis [MESH:C535780] (44)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Cartilage Diseases [MESH:D002357] (438)   Keutel syndrome [MESH:C536167] (102)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Weaver syndrome [MESH:C536687] (16)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Joint Diseases [MESH:D007592] (4657)   Calcification of Joints and Arteries [MESH:C565891] (60)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Ankylosis [MESH:D000844] (479)   Spondylitis, Ankylosing [MESH:D013167] (431)  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)  Spondylitis, Ankylosing [MESH:D013167] (431)  Arthrogryposis [MESH:D001176] (329)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Bruck syndrome 2 [MESH:C537407] (64)  Distal arthrogryposis type 2B [MESH:C538400] (85)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Joint Instability [MESH:D007593] (67)   Arterial Tortuosity Syndrome [MESH:C565942] (12)  Muscular Diseases [MESH:D009135] (4071)   Arthrogryposis [MESH:D001176] (329)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Bruck syndrome 2 [MESH:C537407] (64)  Distal arthrogryposis type 2B [MESH:C538400] (85)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscle Spasticity [MESH:D009128] (187)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Muscular Dystrophy, Oculopharyngeal [MESH:D039141] (32)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 4 [MESH:C538351] (47)  Nemaline Myopathy 7 [MESH:C565198] (21)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Myotonic Disorders [MESH:D020967] (138)   Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Arthrogryposis [MESH:D001176] (329)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Bruck syndrome 2 [MESH:C537407] (64)  Distal arthrogryposis type 2B [MESH:C538400] (85)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Craniofacial Abnormalities [MESH:D019465] (3098)   Weaver syndrome [MESH:C536687] (16)  Larsen syndrome, dominant type [MESH:C537873] (44)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Costello Syndrome [MESH:D056685] (407)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Microcephaly [MESH:D008831] (700)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  VACTERL hydrocephaly [MESH:C536521] (151)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Polydactyly [MESH:D017689] (318)  Proteus Syndrome [MESH:D016715] (152)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Weaver syndrome [MESH:C536687] (16)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Synostosis [MESH:D013580] (817)   Spondylocarpotarsal synostosis [MESH:C535780] (44)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  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)   Bile Duct Neoplasms [MESH:D001650] (367)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Alagille Syndrome [MESH:D016738] (105)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  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)  Hirschsprung Disease [MESH:D006627] (361)  Digestive System Fistula [MESH:D016154] (102)   Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  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)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Stenosis [MESH:D004940] (490)  Esophagitis [MESH:D004941] (1120)  Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Gastroenteritis [MESH:D005759] (4066)   Esophagitis [MESH:D004941] (1120)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Gastrointestinal Stromal Tumors [MESH:D046152] (170)  Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Intestinal Polyposis [MESH:D044483] (1610)   Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Malabsorption Syndromes [MESH:D008286] (492)   Celiac Disease [MESH:D002446] (340)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Duodenal Ulcer [MESH:D004381] (1549)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatorenal Syndrome [MESH:D006530] (910)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Alagille Syndrome [MESH:D016738] (105)  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)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Hepatitis, Animal [MESH:D006520] (260)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis C, Chronic [MESH:D019698] (142)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Liver Cirrhosis [MESH:D008103] (5542)   Cirrhosis, Familial [MESH:C566123] (179)  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)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pancreatitis [MESH:D010195] (1924)   Pancreatitis, Chronic [MESH:D050500] (276)   Hereditary pancreatitis [MESH:C537262] (234)  Tropical Calcific Pancreatitis [MESH:C564276] (33)  Peritoneal Diseases [MESH:D010532] (1119)   Peritoneal Fibrosis [MESH:D056627] (488)  Peritonitis [MESH:D010538] (800) 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)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Larsen syndrome, dominant type [MESH:C537873] (44)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Larsen syndrome, dominant type [MESH:C537873] (44)  Cleft Palate [MESH:D002972] (1330)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Larsen syndrome, dominant type [MESH:C537873] (44)  Cleft Palate [MESH:D002972] (1330)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Tooth Abnormalities [MESH:D014071] (622)   Larsen syndrome, dominant type [MESH:C537873] (44)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Larsen syndrome, dominant type [MESH:C537873] (44)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Granuloma, Respiratory Tract [MESH:D015769] (502)  Respiratory System Abnormalities [MESH:D015619] (243)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Lung Diseases [MESH:D008171] (7249)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Cystic Fibrosis [MESH:D003550] (760)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Hypertension, Pulmonary [MESH:D006976] (2000)   Persistent Fetal Circulation Syndrome [MESH:D010547] (60)   Alveolar capillary dysplasia [MESH:C536590] (56)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Alveolitis, Extrinsic Allergic [MESH:D000542] (496)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Nose Diseases [MESH:D009668] (1504)   Paranasal Sinus Diseases [MESH:D010254] (476)   Sinusitis [MESH:D012852] (469)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Respiratory Insufficiency [MESH:D012131] (841)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)  Hyperventilation [MESH:D006985] (654)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (4098)  Respiratory Tract Fistula [MESH:D016156] (91)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Sinusitis [MESH:D012852] (469)  Pneumonia [MESH:D011014] (3482)   Pneumonia, Aspiration [MESH:D011015] (824)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Tracheal Diseases [MESH:D014133] (107)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  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)  Nose Diseases [MESH:D009668] (1504)   Paranasal Sinus Diseases [MESH:D010254] (476)   Sinusitis [MESH:D012852] (469)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   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)   Autonomic Nervous System Diseases [MESH:D001342] (882)  Chronobiology Disorders [MESH:D021081] (970)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  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)   Hepatolenticular Degeneration [MESH:D006527] (473)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Wernicke Encephalopathy [MESH:D014899] (75)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Leigh Disease [MESH:D007888] (206)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  MERRF Syndrome [MESH:D017243] (1053)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Carbamoyl-Phosphate Synthase I Deficiency Disease [MESH:D020165] (49)  Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Pituitary Apoplexy [MESH:D010899] (125)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212)   Hematoma, Subdural, Acute [MESH:D020199] (63)  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)  Frontotemporal Lobar Degeneration [MESH:D057174] (310)   Frontotemporal Dementia [MESH:D057180] (300)   Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Pick Disease of the Brain [MESH:D020774] (184)  Epilepsy [MESH:D004827] (6274)   Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Spasms, Infantile [MESH:D013036] (468)  Seizures [MESH:D012640] (4502)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Hydrocephalus [MESH:D006849] (276)   VACTERL hydrocephaly [MESH:C536521] (151)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Pituitary Apoplexy [MESH:D010899] (125)  Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1250)   Acromegaly [MESH:D000172] (466)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)   VACTERL hydrocephaly [MESH:C536521] (151)  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)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Encephalitis [MESH:D004660] (226)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Encephalitis [MESH:D004660] (351)   Encephalitis, Viral [MESH:D018792] (183)   Subacute Sclerosing Panencephalitis [MESH:D013344] (63)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Movement Disorders [MESH:D009069] (4823)   Angelman Syndrome [MESH:D017204] (124)  Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Dystonic Disorders [MESH:D020821] (729)   Myoclonic dystonia [MESH:C536096] (245)  Juvenile-onset dystonia [MESH:C537704] (143)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Vestibulocochlear Nerve Diseases [MESH:D000160] (111)   Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Corpus callosum agenesis neuronopathy [MESH:C536446] (20)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  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 4B1 [MESH:C535420] (16)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Dominant Intermediate C [MESH:C564257] (39)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Microcephaly [MESH:D008831] (700)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Neuronal Migration Disorders [MESH:D054081] (264)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Neural Tube Defects [MESH:D009436] (2143)   Meningomyelocele [MESH:D008591] (100)  Spinal Dysraphism [MESH:D016135] (1025)  Nervous System Neoplasms [MESH:D009423] (3073)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neurocutaneous Syndromes [MESH:D020752] (1230)   von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Cockayne Syndrome [MESH:D003057] (107)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 4B1 [MESH:C535420] (16)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Dominant Intermediate C [MESH:C564257] (39)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 7 [MESH:C563989] (10)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)   Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Paresis [MESH:D010291] (419)  Dyskinesias [MESH:D020820] (3365)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Myoclonus [MESH:D009207] (427)  Ataxia [MESH:D001259] (1138)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Episodic Ataxia, Type 1 [MESH:C563278] (21)  Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Korsakoff Syndrome [MESH:D020915] (69)  Intellectual Disability [MESH:D008607] (3054)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mental Retardation, Autosomal Recessive 1 [MESH:C565406] (19)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  De Lange Syndrome [MESH:D003635] (55)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Snyder Robinson syndrome [MESH:C536678] (19)  Lubs X-linked mental retardation syndrome [MESH:C537723] (44)  Mental Retardation, X-Linked 63 [MESH:C564522] (64)  Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Mental Retardation, X-Linked, Syndromic 13 [MESH:C566875] (44)  Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations [MESH:C566878] (44)  Adrenoleukodystrophy [MESH:D000326] (1348)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Neuromuscular Manifestations [MESH:D020879] (2130)   Fasciculation [MESH:D005207] (204)  Muscle Hypotonia [MESH:D009123] (258)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Spasticity [MESH:D009128] (187)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Myokymia [MESH:D020385] (26)   Episodic Ataxia, Type 1 [MESH:C563278] (21)  Spasm [MESH:D013035] (418)   Trismus [MESH:D014313] (221)  Pain [MESH:D010146] (3875)   Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Seizures [MESH:D012640] (4514)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Muscular Diseases [MESH:D009135] (3538)   Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Muscular Dystrophy, Oculopharyngeal [MESH:D039141] (32)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myopathies, Structural, Congenital [MESH:D020914] (272)   Myopathies, Nemaline [MESH:D017696] (173)   Nemaline myopathy 4 [MESH:C538351] (47)  Nemaline Myopathy 7 [MESH:C565198] (21)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Myotonic Disorders [MESH:D020967] (138)   Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Corpus callosum agenesis neuronopathy [MESH:C536446] (20)  Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  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 4B1 [MESH:C535420] (16)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Dominant Intermediate C [MESH:C564257] (39)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Polyradiculoneuropathy [MESH:D011129] (213)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Sleep Apnea Syndromes [MESH:D012891] (570)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212)   Hematoma, Subdural, Acute [MESH:D020199] (63) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76)  Corneal Diseases [MESH:D003316] (1445)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Fuchs' Endothelial Dystrophy [MESH:D005642] (86)   Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)  Corneal Opacity [MESH:D003318] (544)   Peters anomaly [MESH:C537884] (465)  Eye Abnormalities [MESH:D005124] (1233)   Peters anomaly [MESH:C537884] (465)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Coloboma [MESH:D003103] (315)  Fraser Syndrome [MESH:D058497] (29)  Microphthalmos [MESH:D008850] (273)   Nanophthalmos 2 [MESH:C563700] (4)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Fuchs' Endothelial Dystrophy [MESH:D005642] (86)   Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Retinitis Pigmentosa 31 [MESH:C563685] (14)  Cone-Rod Dystrophy 7 [MESH:C566350] (11)  Eye Neoplasms [MESH:D005134] (413)   Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Hyperferritinemia, hereditary, with congenital cataracts [MESH:C538137] (82)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma 3, Primary Congenital, A [MESH:C565547] (434)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Glaucoma, Open-Angle [MESH:D005902] (1281)   Glaucoma, Primary Open Angle [MESH:C562750] (466)  Glaucoma 1, Open Angle, A [MESH:C564234] (446)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)  Refractive Errors [MESH:D012030] (457)   Anisometropia [MESH:D015858] (152)  Myopia [MESH:D009216] (349)  Retinal Diseases [MESH:D012164] (3747)   Retinitis [MESH:D012173] (137)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Fundus Dystrophy, Pseudoinflammatory, Of Sorsby [MESH:C564992] (121)  Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Retinitis Pigmentosa 31 [MESH:C563685] (14)  Cone-Rod Dystrophy 7 [MESH:C566350] (11)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Uveal Diseases [MESH:D014603] (2428)   Uveal Neoplasms [MESH:D014604] (115)   Uveal melanoma [MESH:C536494] (109)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) 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)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)  Penile Diseases [MESH:D010409] (1805)   Penile Induration [MESH:D010411] (495)  Penile Neoplasms [MESH:D010412] (890)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  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)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)  Urogenital Abnormalities [MESH:D014564] (2065)   Cryptorchidism [MESH:D003456] (215)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Kallmann Syndrome [MESH:D017436] (147)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  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)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  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)   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  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Uterine Diseases [MESH:D014591] (2479)   Endometrial Hyperplasia [MESH:D004714] (263)  Uterine Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Abnormalities [MESH:D014564] (2043)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Kallmann Syndrome [MESH:D017436] (147)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  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)  Uterine Cervical Neoplasms [MESH:D002583] (978)  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)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  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)   Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Fetal Death [MESH:D005313] (464)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Prenatal Injuries [MESH:D049188] (1314)  Diabetes, Gestational [MESH:D016640] (1157)   Fetal Macrosomia [MESH:D005320] (20)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Fetal Diseases [MESH:D005315] (1206)   Chorioamnionitis [MESH:D002821] (313)  Fetal Growth Retardation [MESH:D005317] (986)  Fetal Macrosomia [MESH:D005320] (20)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Fetal Membranes, Premature Rupture [MESH:D005322] (356)   Chorioamnionitis [MESH:D002821] (313)  Placenta Diseases [MESH:D010922] (1781)   Chorioamnionitis [MESH:D002821] (313)  Pregnancy in Diabetics [MESH:D011254] (22)   Fetal Macrosomia [MESH:D005320] (20)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16) 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)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VACTERL hydrocephaly [MESH:C536521] (151)  Alagille Syndrome [MESH:D016738] (105)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)  Tetralogy of Fallot [MESH:D013771] (121)  Ductus Arteriosus, Patent [MESH:D004374] (325)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)   Atrial Septal Defect 4 [MESH:C566963] (13)  Atrial Septal Defect 5 [MESH:C567561] (51)  Vascular Malformations [MESH:D054079] (1098)   Arterial Tortuosity Syndrome [MESH:C565942] (12)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Heart Diseases [MESH:D006331] (8614)   Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Cardiac Conduction Defect [MESH:C562490] (16)  Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 4 [MESH:C567508] (21)  Brugada Syndrome 3 [MESH:C567509] (44)  Long QT Syndrome [MESH:D008133] (693)   Timothy syndrome [MESH:C536962] (44)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Cardiomegaly [MESH:D006332] (4081)   Cantu syndrome [MESH:C535572] (42)  Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1D [MESH:C563306] (50)  Cardiomyopathy, Dilated, 1C [MESH:C563307] (20)  Cardiomyopathy, Dilated, 1o [MESH:C563906] (42)  Cardiomyopathy, Dilated, 1x [MESH:C566907] (9)  Cardiomyopathy, Dilated, 1w [MESH:C566954] (66)  Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathies [MESH:D009202] (5331)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1D [MESH:C563306] (50)  Cardiomyopathy, Dilated, 1C [MESH:C563307] (20)  Cardiomyopathy, Dilated, 1o [MESH:C563906] (42)  Cardiomyopathy, Dilated, 1x [MESH:C566907] (9)  Cardiomyopathy, Dilated, 1w [MESH:C566954] (66)  Cardiomyopathy, Dilated, 1y [MESH:C567507] (103)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Cardiomyopathy, Familial Hypertrophic, 2 [MESH:C566171] (50)  Cardiomyopathy, Familial Hypertrophic, 11 [MESH:C567419] (51)  Cardiomyopathy, Familial Hypertrophic, 15 [MESH:C567681] (66)  Cardiomyopathy, Restrictive [MESH:D002313] (94)   Cardiomyopathy, Familial Restrictive, 3 [MESH:C567316] (50)  Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VACTERL hydrocephaly [MESH:C536521] (151)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)  Tetralogy of Fallot [MESH:D013771] (121)  Ductus Arteriosus, Patent [MESH:D004374] (325)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)   Atrial Septal Defect 4 [MESH:C566963] (13)  Atrial Septal Defect 5 [MESH:C567561] (51)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   Keutel syndrome [MESH:C536167] (102)  LEOPARD Syndrome [MESH:D044542] (299)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial 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 Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  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)  Pulmonary Valve Stenosis [MESH:D011666] (109)   Keutel syndrome [MESH:C536167] (102)  Vascular Diseases [MESH:D014652] (8691)   Calcification of Joints and Arteries [MESH:C565891] (60)  Diabetic Angiopathies [MESH:D003925] (1984)  Hyperemia [MESH:D006940] (2372)  Hypotension [MESH:D007022] (4045)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Coronary Aneurysm [MESH:D003323] (204)  Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  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)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Pituitary Apoplexy [MESH:D010899] (125)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212)   Hematoma, Subdural, Acute [MESH:D020199] (63)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)  Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Occipital horn syndrome [MESH:C537860] (58)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  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 Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Myocardial Stunning [MESH:D017682] (1816)  No-Reflow Phenomenon [MESH:D054318] (277)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784)  Cogan Syndrome [MESH:D055952] (78)   Corneal dystrophy, epithelial basement membrane [MESH:C535477] (76) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  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, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Anemia, Hemolytic [MESH:D000743] (3083)   Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to [MESH:C565557] (312)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Elliptocytosis, Hereditary [MESH:D004612] (95)   Elliptocytosis 1 [MESH:C567520] (9)  Spherocytosis, Hereditary [MESH:D013103] (137)   Spherocytosis, Type 1 [MESH:C567159] (21)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  Anemia, Sideroblastic [MESH:D000756] (636)   X-linked sideroblastic anemia [MESH:C536761] (58)  Red-Cell Aplasia, Pure [MESH:D012010] (183)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Thrombocythemia, Essential [MESH:D013920] (707)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Antithrombin III Deficiency [MESH:D020152] (80)  Factor VII Deficiency [MESH:D005168] (61)  Hemophilia A [MESH:D006467] (58)  Hemophilia B [MESH:D002836] (24)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  von Willebrand Diseases [MESH:D014842] (75)   von Willebrand Disease, Type 1 [MESH:D056725] (67)  von Willebrand Disease, Type 2 [MESH:D056728] (67)  von Willebrand Disease, Type 3 [MESH:D056729] (67)  Coagulation Protein Disorders [MESH:D020147] (580)   Factor VII Deficiency [MESH:D005168] (61)  Hemophilia A [MESH:D006467] (58)  Hemophilia B [MESH:D002836] (24)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  von Willebrand Diseases [MESH:D014842] (75)   von Willebrand Disease, Type 1 [MESH:D056725] (67)  von Willebrand Disease, Type 2 [MESH:D056728] (67)  von Willebrand Disease, Type 3 [MESH:D056729] (67)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Antithrombin III Deficiency [MESH:D020152] (80)  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)  Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Sideroblastic [MESH:D000756] (636)   X-linked sideroblastic anemia [MESH:C536761] (58)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Factor VII Deficiency [MESH:D005168] (61)  Hemophilia A [MESH:D006467] (58)  Hemophilia B [MESH:D002836] (24)  Thrombocythemia, Essential [MESH:D013920] (707)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Occipital horn syndrome [MESH:C537860] (58)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Hemangioma, Cavernous [MESH:D006392] (38)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  von Willebrand Diseases [MESH:D014842] (75)   von Willebrand Disease, Type 1 [MESH:D056725] (67)  von Willebrand Disease, Type 2 [MESH:D056728] (67)  von Willebrand Disease, Type 3 [MESH:D056729] (67)  Leukocyte Disorders [MESH:D007960] (2662)   Leukostasis [MESH:D018921] (769)  Eosinophilia [MESH:D004802] (537)   Hypereosinophilic Syndrome [MESH:D017681] (119)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Chediak-Higashi Syndrome [MESH:D002609] (21)  Thrombophilia [MESH:D019851] (592)   Thrombophilia, X-Linked, Due To Factor Ix Defect [MESH:C567581] (24)  Antithrombin III Deficiency [MESH:D020152] (80)  Disseminated Intravascular Coagulation [MESH:D004211] (462)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphedema [MESH:D008209] (162)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, T-Cell [MESH:D016399] (1204)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Spondylocarpotarsal synostosis [MESH:C535780] (44)  Keutel syndrome [MESH:C536167] (102)  Weaver syndrome [MESH:C536687] (16)  Ulnar-mammary syndrome [MESH:C536937] (57)  Bamforth syndrome [MESH:C537901] (186)  Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)  Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12)  Alagille Syndrome [MESH:D016738] (105)  Angelman Syndrome [MESH:D017204] (124)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  Cockayne Syndrome [MESH:D003057] (107)  Costello Syndrome [MESH:D056685] (407)  De Lange Syndrome [MESH:D003635] (55)  Fraser Syndrome [MESH:D058497] (29)  LEOPARD Syndrome [MESH:D044542] (299)  Proteus Syndrome [MESH:D016715] (152)  Sotos Syndrome [MESH:D058495] (39)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  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)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  VACTERL hydrocephaly [MESH:C536521] (151)  Alagille Syndrome [MESH:D016738] (105)  Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)  Tetralogy of Fallot [MESH:D013771] (121)  Ductus Arteriosus, Patent [MESH:D004374] (325)   Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)  Heart Septal Defects [MESH:D006343] (385)   Heart Septal Defects, Atrial [MESH:D006344] (209)   Atrial Septal Defect 4 [MESH:C566963] (13)  Atrial Septal Defect 5 [MESH:C567561] (51)  Long QT Syndrome [MESH:D008133] (693)   Timothy syndrome [MESH:C536962] (44)  Vascular Malformations [MESH:D054079] (1108)   Arterial Tortuosity Syndrome [MESH:C565942] (12)  Chromosome Disorders [MESH:D025063] (2030)   Angelman Syndrome [MESH:D017204] (124)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  De Lange Syndrome [MESH:D003635] (55)  Sotos Syndrome [MESH:D058495] (39)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)  Eye Abnormalities [MESH:D005124] (1233)   Peters anomaly [MESH:C537884] (465)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Coloboma [MESH:D003103] (315)  Fraser Syndrome [MESH:D058497] (29)  Microphthalmos [MESH:D008850] (273)   Nanophthalmos 2 [MESH:C563700] (4)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Arthrogryposis [MESH:D001176] (329)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Bruck syndrome 2 [MESH:C537407] (64)  Distal arthrogryposis type 2B [MESH:C538400] (85)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Craniofacial Abnormalities [MESH:D019465] (3064)   Weaver syndrome [MESH:C536687] (16)  Larsen syndrome, dominant type [MESH:C537873] (44)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Microcephaly [MESH:D008831] (700)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  VACTERL hydrocephaly [MESH:C536521] (151)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Polydactyly [MESH:D017689] (318)  Proteus Syndrome [MESH:D016715] (152)  Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Weaver syndrome [MESH:C536687] (16)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Synostosis [MESH:D013580] (817)   Spondylocarpotarsal synostosis [MESH:C535780] (44)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Syndactyly [MESH:D013576] (487)   Timothy syndrome [MESH:C536962] (44)  Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Corpus callosum agenesis neuronopathy [MESH:C536446] (20)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Hemangioma, Cavernous, Central Nervous System [MESH:D020786] (35)  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 4B1 [MESH:C535420] (16)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Dominant Intermediate C [MESH:C564257] (39)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Microcephaly [MESH:D008831] (700)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Neuronal Migration Disorders [MESH:D054081] (264)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Neural Tube Defects [MESH:D009436] (2143)   Meningomyelocele [MESH:D008591] (100)  Spinal Dysraphism [MESH:D016135] (1025)  Skin Abnormalities [MESH:D012868] (1723)   Acrodermatitis [MESH:D000169] (56)   Acrodermatitis enteropathica [MESH:C538178] (51)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Occipital horn syndrome [MESH:C537860] (58)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosis [MESH:D007057] (481)   Ichthyosis Vulgaris [MESH:D016112] (27)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Larsen syndrome, dominant type [MESH:C537873] (44)  Cleft Palate [MESH:D002972] (1330)   Larsen syndrome, dominant type [MESH:C537873] (44)  Bamforth syndrome [MESH:C537901] (186)  Tooth Abnormalities [MESH:D014071] (622)   Larsen syndrome, dominant type [MESH:C537873] (44)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Urogenital Abnormalities [MESH:D014564] (2064)   Cryptorchidism [MESH:D003456] (215)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Kallmann Syndrome [MESH:D017436] (147)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Fetal Diseases [MESH:D005315] (1205)   Chorioamnionitis [MESH:D002821] (313)  Fetal Growth Retardation [MESH:D005317] (986)  Fetal Macrosomia [MESH:D005320] (20)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Genetic Diseases, Inborn [MESH:D030342] (9766)   ACTH Deficiency, Isolated [MESH:C562707] (124)  Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Cirrhosis, Familial [MESH:C566123] (179)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Alagille Syndrome [MESH:D016738] (105)  alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Costello Syndrome [MESH:D056685] (407)  Cystic Fibrosis [MESH:D003550] (760)  Kallmann Syndrome [MESH:D017436] (147)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Elliptocytosis, Hereditary [MESH:D004612] (95)   Elliptocytosis 1 [MESH:C567520] (9)  Spherocytosis, Hereditary [MESH:D013103] (137)   Spherocytosis, Type 1 [MESH:C567159] (21)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Antithrombin III Deficiency [MESH:D020152] (80)  Factor VII Deficiency [MESH:D005168] (61)  Hemophilia A [MESH:D006467] (58)  Hemophilia B [MESH:D002836] (24)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  von Willebrand Diseases [MESH:D014842] (75)   von Willebrand Disease, Type 1 [MESH:D056725] (67)  von Willebrand Disease, Type 2 [MESH:D056728] (67)  von Willebrand Disease, Type 3 [MESH:D056729] (67)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 4 [MESH:C567508] (21)  Brugada Syndrome 3 [MESH:C567509] (44)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Cardiomyopathy, Familial Hypertrophic, 3 [MESH:C566170] (103)  Cardiomyopathy, Familial Hypertrophic, 2 [MESH:C566171] (50)  Cardiomyopathy, Familial Hypertrophic, 11 [MESH:C567419] (51)  Cardiomyopathy, Familial Hypertrophic, 15 [MESH:C567681] (66)  Chromosome Disorders [MESH:D025063] (2030)   Angelman Syndrome [MESH:D017204] (124)  Beckwith-Wiedemann Syndrome [MESH:D001506] (193)  De Lange Syndrome [MESH:D003635] (55)  Sotos Syndrome [MESH:D058495] (39)  Dwarfism [MESH:D004392] (783)   Boomerang dysplasia [MESH:C536573] (44)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12)  Cockayne Syndrome [MESH:D003057] (107)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1A [MESH:C536015] (16)  Congenital Hypothyroidism [MESH:D003409] (266)   Weaver syndrome [MESH:C536687] (16)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal dystrophy Avellino type [MESH:C535474] (76)  Corneal dystrophy of Bowman layer, type 1 [MESH:C535476] (76)  Corneal dystrophy, Thiel-Behnke type [MESH:C535942] (76)  Groenouw type I corneal dystrophy [MESH:C537304] (76)  Lattice corneal dystrophy type 1 [MESH:C537881] (76)  Corneal Dystrophy, Posterior Polymorphous, 3 [MESH:C563788] (60)  Corneal Dystrophy, Lattice Type IIIA [MESH:C563923] (76)  Fuchs' Endothelial Dystrophy [MESH:D005642] (86)   Corneal Dystrophy, Fuchs Endothelial, 6 [MESH:C567675] (60)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Retinitis Pigmentosa 31 [MESH:C563685] (14)  Cone-Rod Dystrophy 7 [MESH:C566350] (11)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Arthrogryposis multiplex congenita, distal, X-linked [MESH:C535380] (27)  Cantu syndrome [MESH:C535572] (42)  X-linked sideroblastic anemia [MESH:C536761] (58)  Spinal Muscular Atrophy, Distal, X-Linked 3 [MESH:C564506] (58)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Thrombophilia, X-Linked, Due To Factor Ix Defect [MESH:C567581] (24)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Hemophilia B [MESH:D002836] (24)  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)   Snyder Robinson syndrome [MESH:C536678] (19)  Lubs X-linked mental retardation syndrome [MESH:C537723] (44)  Mental Retardation, X-Linked 63 [MESH:C564522] (64)  Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Mental Retardation, X-Linked, Syndromic 13 [MESH:C566875] (44)  Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations [MESH:C566878] (44)  Adrenoleukodystrophy [MESH:D000326] (1348)  Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Cockayne Syndrome [MESH:D003057] (107)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 4B1 [MESH:C535420] (16)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth Disease, Dominant Intermediate C [MESH:C564257] (39)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 10, autosomal dominant [MESH:C537482] (20)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Snyder Robinson syndrome [MESH:C536678] (19)  Lubs X-linked mental retardation syndrome [MESH:C537723] (44)  Mental Retardation, X-Linked 63 [MESH:C564522] (64)  Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Mental Retardation, X-Linked, Syndromic 13 [MESH:C566875] (44)  Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations [MESH:C566878] (44)  Adrenoleukodystrophy [MESH:D000326] (1348)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Rett Syndrome [MESH:D015518] (143)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 7 [MESH:C563989] (10)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Loeys-Dietz Syndrome [MESH:D055947] (263)   Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Malonic aciduria [MESH:C535702] (31)  Butyrylcholinesterase deficiency [MESH:C537417] (176)  Coumarin Resistance [MESH:C563039] (397)  Mitochondrial Complex II Deficiency [MESH:C565375] (66)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  Porphyrias [MESH:D011164] (917)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutamine deficiency, congenital [MESH:C536832] (117)  Methylmalonic acidemia [MESH:C537358] (764)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Hyperhomocysteinemia [MESH:D020138] (1724)  Maple Syrup Urine Disease [MESH:D008375] (127)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Carbamoyl-Phosphate Synthase I Deficiency Disease [MESH:D020165] (49)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Leigh Disease [MESH:D007888] (206)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  MERRF Syndrome [MESH:D017243] (1053)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Carbamoyl-Phosphate Synthase I Deficiency Disease [MESH:D020165] (49)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Transaldolase Deficiency [MESH:C563207] (61)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease XII [MESH:C562718] (98)  Glycogen Storage Disease XIII [MESH:C567861] (52)  Glycogen Storage Disease Type III [MESH:D006010] (39)  Glycogen Storage Disease Type V [MESH:D006012] (165)  Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis IV [MESH:D009085] (46)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Leigh Disease [MESH:D007888] (206)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 7 [MESH:C563989] (10)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis IV [MESH:D009085] (46)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Purine Nucleoside Phosphorylase Deficiency [MESH:C562587] (63)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Mineralocorticoid Excess Syndrome, Apparent [MESH:D043204] (121)   Apparent mineralocorticoid excess [MESH:C537422] (120)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular dystrophy congenital, merosin negative [MESH:C537384] (34)  Distal Myopathies [MESH:D049310] (178)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Muscular Dystrophy, Oculopharyngeal [MESH:D039141] (32)  Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)   Sarcoglycanopathies [MESH:D058088] (49)   Limb-girdle muscular dystrophy, type 2E [MESH:C535902] (24)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Turcot syndrome [MESH:C536928] (159)  Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Wilms Tumor [MESH:D009396] (553)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Bruck syndrome 2 [MESH:C537407] (64)  Skin Diseases, Genetic [MESH:D012873] (3456)   dowling-degos disease [MESH:C562924] (53)  Arterial Tortuosity Syndrome [MESH:C565942] (12)  Darier Disease [MESH:D007644] (125)  Ichthyosis Vulgaris [MESH:D016112] (27)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Cutis Laxa [MESH:D003483] (177)   Occipital horn syndrome [MESH:C537860] (58)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Atopic, 2 [MESH:C565293] (26)  Dermatitis, Atopic, 1 [MESH:C566404] (26)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Occipital horn syndrome [MESH:C537860] (58)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (259)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Cystic Fibrosis [MESH:D003550] (760)  Hyperostosis, Cortical, Congenital [MESH:D006958] (392)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Jaundice, Neonatal [MESH:D007567] (290)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Ichthyosis [MESH:D007057] (476)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Infant, Premature, Diseases [MESH:D007235] (1292)   Respiratory Distress Syndrome, Newborn [MESH:D012127] (169)  Persistent Fetal Circulation Syndrome [MESH:D010547] (60)   Alveolar capillary dysplasia [MESH:C536590] (56) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Noonan Syndrome [MESH:D009634] (506)  Penile Induration [MESH:D010411] (495)  Scleroderma, Localized [MESH:D012594] (1597)  Cartilage Diseases [MESH:D002357] (438)   Keutel syndrome [MESH:C536167] (102)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Occipital horn syndrome [MESH:C537860] (58)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Osteogenesis Imperfecta [MESH:D010013] (481)   Osteogenesis imperfecta, type 2A [MESH:C536042] (375)  Osteogenesis imperfecta, type 3 [MESH:C536044] (375)  Osteogenesis imperfecta, type 4 [MESH:C536045] (375)  Bruck syndrome 2 [MESH:C537407] (64)  Cutis Laxa [MESH:D003483] (177)   Occipital horn syndrome [MESH:C537860] (58)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Mucinoses [MESH:D017520] (177)   Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis IV [MESH:D009085] (46)  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)   Dermatomyositis [MESH:D003882] (1826)  Lipomatosis [MESH:D008068] (182)  Mastocytosis [MESH:D008415] (60)  Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Scleroderma, Localized [MESH:D012594] (1597)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Ulnar-mammary syndrome [MESH:C536937] (57)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Dermatitis [MESH:D003872] (4530)   Eczema [MESH:D004485] (235)  Acrodermatitis [MESH:D000169] (56)   Acrodermatitis enteropathica [MESH:C538178] (51)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Atopic, 2 [MESH:C565293] (26)  Dermatitis, Atopic, 1 [MESH:C566404] (26)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Bamforth syndrome [MESH:C537901] (186)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136)  Hypertrichosis [MESH:D006983] (97)   Cantu syndrome [MESH:C535572] (42)  Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Keratoacanthoma [MESH:D007636] (83)   Keratoacanthoma familial [MESH:C536150] (78)  Keratosis [MESH:D007642] (1941)   Darier Disease [MESH:D007644] (125)  Keratosis, Seborrheic [MESH:D017492] (64)  Ichthyosis [MESH:D007057] (481)   Ichthyosis Vulgaris [MESH:D016112] (27)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Panniculitis [MESH:D015434] (88)   Panniculitis, Nodular Nonsuppurative [MESH:D010201] (78)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   dowling-degos disease [MESH:C562924] (53)  Melanosis [MESH:D008548] (459)   Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)  Hypopigmentation [MESH:D017496] (718)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Skin Abnormalities [MESH:D012868] (1709)   Acrodermatitis [MESH:D000169] (56)   Acrodermatitis enteropathica [MESH:C538178] (51)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Occipital horn syndrome [MESH:C537860] (58)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosis [MESH:D007057] (481)   Ichthyosis Vulgaris [MESH:D016112] (27)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Eczema [MESH:D004485] (235)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Atopic, 2 [MESH:C565293] (26)  Dermatitis, Atopic, 1 [MESH:C566404] (26)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Dermatitis, Occupational [MESH:D009783] (311)  Skin Diseases, Genetic [MESH:D012873] (3481)   dowling-degos disease [MESH:C562924] (53)  Arterial Tortuosity Syndrome [MESH:C565942] (12)  Darier Disease [MESH:D007644] (125)  Ichthyosis Vulgaris [MESH:D016112] (27)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Cutis Laxa [MESH:D003483] (177)   Occipital horn syndrome [MESH:C537860] (58)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Atopic, 2 [MESH:C565293] (26)  Dermatitis, Atopic, 1 [MESH:C566404] (26)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152)  Occipital horn syndrome [MESH:C537860] (58)  Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)   Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis [MESH:C564367] (84)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Skin Diseases, Infectious [MESH:D012874] (2684)   Dermatomycoses [MESH:D003881] (267)   Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224)  Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)  Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   dowling-degos disease [MESH:C562924] (53)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)  Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Blister [MESH:D001768] (93)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis Bullosa Simplex [MESH:D016110] (140)   Epidermolysis bullosa simplex with mottled pigmentation [MESH:C535959] (53)  Epidermolysis Bullosa Simplex with Migratory Circinate Erythema [MESH:C563730] (53)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Skin Neoplasms [MESH:D012878] (2991)   Nevus, Epidermal [MESH:C562736] (112) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Z. Exceptions (817)   Not Fully Specified [NFS] (817)  Metabolic Diseases [MESH:D008659] (9025)   Porphyrias [MESH:D011164] (917)  Acid-Base Imbalance [MESH:D000137] (854)   Acidosis [MESH:D000138] (626)   Succinyl-CoA:3-oxoacid CoA transferase deficiency [MESH:C537527] (38)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Wernicke Encephalopathy [MESH:D014899] (75)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Leigh Disease [MESH:D007888] (206)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  MERRF Syndrome [MESH:D017243] (1053)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Carbamoyl-Phosphate Synthase I Deficiency Disease [MESH:D020165] (49)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Keutel syndrome [MESH:C536167] (102)  Aortic Valve, Calcification of [MESH:C562942] (655)  Tropical Calcific Pancreatitis [MESH:C564276] (33)  Calcification of Joints and Arteries [MESH:C565891] (60)  Vascular Calcification [MESH:D061205] (138)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Cockayne Syndrome [MESH:D003057] (107)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)  Fanconi Anemia [MESH:D005199] (1604)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Maturity-Onset Diabetes of the Young, Type 7 [MESH:C566466] (32)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)  Hypoglycemia [MESH:D007003] (2420)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  ACTH Deficiency, Isolated [MESH:C562707] (124)  Iron Metabolism Disorders [MESH:D019189] (2139)   Hyperferritinemia, hereditary, with congenital cataracts [MESH:C538137] (82)  Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipomatosis [MESH:D008068] (182)  Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hypertriglyceridemia [MESH:D015228] (808)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (409)   Hypobetalipoproteinemias [MESH:D006995] (181)   Hypobetalipoproteinemia, Familial, Apolipoprotein B [MESH:D052476] (131)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 7 [MESH:C563989] (10)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Malabsorption Syndromes [MESH:D008286] (1869)   Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Malonic aciduria [MESH:C535702] (31)  Butyrylcholinesterase deficiency [MESH:C537417] (176)  Coumarin Resistance [MESH:C563039] (397)  Mitochondrial Complex II Deficiency [MESH:C565375] (66)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  Porphyrias [MESH:D011164] (917)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutamine deficiency, congenital [MESH:C536832] (117)  Methylmalonic acidemia [MESH:C537358] (764)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Hyperhomocysteinemia [MESH:D020138] (1724)  Maple Syrup Urine Disease [MESH:D008375] (127)  Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Carbamoyl-Phosphate Synthase I Deficiency Disease [MESH:D020165] (49)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Leigh Disease [MESH:D007888] (206)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  MERRF Syndrome [MESH:D017243] (1053)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Carbamoyl-Phosphate Synthase I Deficiency Disease [MESH:D020165] (49)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Transaldolase Deficiency [MESH:C563207] (61)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease XII [MESH:C562718] (98)  Glycogen Storage Disease XIII [MESH:C567861] (52)  Glycogen Storage Disease Type III [MESH:D006010] (39)  Glycogen Storage Disease Type V [MESH:D006012] (165)  Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis IV [MESH:D009085] (46)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Leigh Disease [MESH:D007888] (206)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 7 [MESH:C563989] (10)  Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidosis, GM1 [MESH:D016537] (40)  Mucopolysaccharidoses [MESH:D009083] (164)   Mucopolysaccharidosis IV [MESH:D009085] (46)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Menkes Kinky Hair Syndrome [MESH:D007706] (60)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Purine Nucleoside Phosphorylase Deficiency [MESH:C562587] (63)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Mineralocorticoid Excess Syndrome, Apparent [MESH:D043204] (121)   Apparent mineralocorticoid excess [MESH:C537422] (120)  Mitochondrial Diseases [MESH:D028361] (2561)   Mitochondrial Complex II Deficiency [MESH:C565375] (66)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Carbamoyl-Phosphate Synthase I Deficiency Disease [MESH:D020165] (49)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Leigh Disease [MESH:D007888] (206)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 10 [MESH:C567429] (36)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Frontotemporal Lobar Degeneration [MESH:D057174] (308)   Frontotemporal Dementia [MESH:D057180] (298)   Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)  Lipodystrophy [MESH:D008060] (930)   Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy [MESH:C536329] (61)  Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hypokalemia [MESH:D007008] (1041)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)  Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Thiamine Deficiency [MESH:D013832] (139)   Wernicke Encephalopathy [MESH:D014899] (75)  Vitamin E Deficiency [MESH:D014811] (274)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Obesity, Abdominal [MESH:D056128] (115)  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)   ACTH Deficiency, Isolated [MESH:C562707] (124)  Bone Diseases, Endocrine [MESH:D001849] (173)  Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Cushing Syndrome [MESH:D003480] (282)  Diabetes Mellitus [MESH:D003920] (6159)   Maturity-Onset Diabetes of the Young, Type 7 [MESH:C566466] (32)  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 Angiopathies [MESH:D003925] (1984)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Fetal Macrosomia [MESH:D005320] (20)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  Dwarfism [MESH:D004392] (698)   Boomerang dysplasia [MESH:C536573] (44)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12)  Congenital Hypothyroidism [MESH:D003409] (266)   Weaver syndrome [MESH:C536687] (16)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia, Type IV [MESH:C567059] (297)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroid cancer, papillary [MESH:C536915] (111)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Delayed [MESH:D011628] (449)  Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Kallmann Syndrome [MESH:D017436] (147)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Hypogonadism [MESH:D007006] (1123)   Kallmann Syndrome [MESH:D017436] (147)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Cryptorchidism [MESH:D003456] (215)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Apoplexy [MESH:D010899] (125)  Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)  Hypothyroidism [MESH:D007037] (496)   Bamforth syndrome [MESH:C537901] (186)  Congenital Hypothyroidism [MESH:D003409] (266)   Weaver syndrome [MESH:C536687] (16)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, anaplastic [MESH:C536910] (489)  Thyroid cancer, papillary [MESH:C536915] (111) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   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)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   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)   Urticaria [MESH:D014581] (2668)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Atopic, 2 [MESH:C565293] (26)  Dermatitis, Atopic, 1 [MESH:C566404] (26)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Ige Responsiveness, Atopic [MESH:C564133] (267)  Alveolitis, Extrinsic Allergic [MESH:D000542] (495)  Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Chediak-Higashi Syndrome [MESH:D002609] (22)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, T-Cell [MESH:D016399] (1382)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  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)   Blister [MESH:D001768] (93)  Ventricular Remodeling [MESH:D020257] (686)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Corpus callosum agenesis neuronopathy [MESH:C536446] (20)  Alopecia [MESH:D000505] (1383)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Fistula [MESH:D005402] (130)   Digestive System Fistula [MESH:D016154] (102)   Esophageal Fistula [MESH:D004937] (89)   Tracheoesophageal Fistula [MESH:D014138] (88)   Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  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)   Cantu syndrome [MESH:C535572] (42)  Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)   Colonic Polyps [MESH:D003111] (210)  Prolapse [MESH:D011391] (60)   Pelvic Organ Prolapse [MESH:D056887] (59)  Pathologic Processes [MESH:D010335] (9863)   Gliosis [MESH:D005911] (1419)  Hyperammonemia [MESH:D022124] (322)  Hyperbilirubinemia [MESH:D006932] (1860)  Hyperplasia [MESH:D006965] (2463)  Metaplasia [MESH:D008679] (1469)  Necrosis [MESH:D009336] (4019)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Ulcer [MESH:D014456] (392)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Cardiac Conduction Defect [MESH:C562490] (16)  Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Long QT Syndrome [MESH:D008133] (691)   Timothy syndrome [MESH:C536962] (44)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Translocation, Genetic [MESH:D014178] (557)  Death [MESH:D003643] (1328)   Fetal Death [MESH:D005313] (464)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Boomerang dysplasia [MESH:C536573] (44)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Macrocephaly Autism Syndrome [MESH:C565342] (151)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12)  Emphysema [MESH:D004646] (1096)   Subcutaneous Emphysema [MESH:D013352] (82)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Fibrosis [MESH:D005355] (3133)   Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452)  Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Granuloma [MESH:D006099] (587)   Granuloma, Plasma Cell [MESH:D006104] (58)  Granuloma, Respiratory Tract [MESH:D015769] (502)  Growth Disorders [MESH:D006130] (2438)   Omodysplasia type 1 [MESH:C537746] (13)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)  Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Hematuria [MESH:D006417] (477)  Shock, Hemorrhagic [MESH:D012771] (2042)  Hematoma [MESH:D006406] (281)   Hematoma, Subdural [MESH:D006408] (215)   Hematoma, Subdural, Acute [MESH:D020199] (63)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Hematoma, Subdural [MESH:D006408] (212)   Hematoma, Subdural, Acute [MESH:D020199] (63)  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)  Ischemia [MESH:D007511] (3049)   No-Reflow Phenomenon [MESH:D054318] (277)  Neoplastic Processes [MESH:D009385] (5317)   Anaplasia [MESH:D000708] (348)  Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Feminization [MESH:D005262] (655)  Flushing [MESH:D005483] (506)  Reticulocytosis [MESH:D045262] (514)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Birth Weight [MESH:D001724] (377)   Fetal Macrosomia [MESH:D005320] (20)   Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor [MESH:C536399] (16)  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)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12)  Neurologic Manifestations [MESH:D009461] (8702)   Paresis [MESH:D010291] (419)  Dyskinesias [MESH:D020820] (3285)   Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Myoclonus [MESH:D009207] (263)  Ataxia [MESH:D001259] (984)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Episodic Ataxia, Type 1 [MESH:C563278] (21)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Korsakoff Syndrome [MESH:D020915] (69)  Intellectual Disability [MESH:D008607] (1476)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mental Retardation, Autosomal Recessive 1 [MESH:C565406] (19)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Neuromuscular Manifestations [MESH:D020879] (2130)   Fasciculation [MESH:D005207] (204)  Muscle Hypotonia [MESH:D009123] (258)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Spasticity [MESH:D009128] (187)   Spastic ataxia Charlevoix-Saguenay type [MESH:C536787] (37)  Myokymia [MESH:D020385] (26)   Episodic Ataxia, Type 1 [MESH:C563278] (21)  Spasm [MESH:D013035] (418)   Trismus [MESH:D014313] (221)  Pain [MESH:D010146] (3869)   Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 [MESH:C567768] (50)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Seizures [MESH:D012640] (4502)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Hearing Loss, Noise-Induced [MESH:D006317] (134)  Hearing Loss, Central [MESH:D006313] (140)   Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  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)   Anorexia [MESH:D000855] (854)  Diarrhea [MESH:D003967] (858)  Nausea [MESH:D009325] (2300)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Apnea [MESH:D001049] (415)  Respiratory Sounds [MESH:D012135] (713)  Hyperventilation [MESH:D006985] (652)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Skin Manifestations [MESH:D012877] (1250)   Livedo Reticularis [MESH:D054068] (228)   Aortic Aneurysm, Familial Thoracic 6 [MESH:C567085] (221)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  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)   Dermatitis, Occupational [MESH:D009783] (311)  Pneumoconiosis [MESH:D011009] (2670)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Manganese Poisoning [MESH:D020149] (2214)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Wernicke Encephalopathy [MESH:D014899] (75)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Alcohol-Induced Disorders, Nervous System [MESH:D020268] (128)   Alcohol Amnestic Disorder [MESH:D000425] (71)   Korsakoff Syndrome [MESH:D020915] (69)  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)  Fractures, Bone [MESH:D050723] (597)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (217)   Hematoma, Subdural [MESH:D006408] (212)   Hematoma, Subdural, Acute [MESH:D020199] (63)  Dislocations [MESH:D004204] (62)   Larsen syndrome, dominant type [MESH:C537873] (44)  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)   Heart Injuries [MESH:D006335] (82)  Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212)   Hematoma, Subdural, Acute [MESH:D020199] (63) D01. Inorganic Chemicals  D01. Inorganic Chemicals  Arsenicals [MESH:D001152] (159)   Arsenates [MESH:D001149] (17)  Electrolytes [MESH:D004573] (1605)   Ions [MESH:D007477] (1589)   Anions [MESH:D000838] (1583)   Arsenates [MESH:D001149] (17) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Organometallic Compounds [MESH:D009942] (4369)   Arsenicals [MESH:D001152] (190)   Arsenates [MESH:D001149] (17) 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)  Physical Examination [MESH:D010808] (1041)   Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Boomerang dysplasia [MESH:C536573] (44)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Macrocephaly Autism Syndrome [MESH:C565342] (151)  Trichorhinophalangeal Syndrome, Type III [MESH:C566033] (24)  Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mental Retardation, Autosomal Recessive 1 [MESH:C565406] (19)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Psychomotor Disorders [MESH:D011596] (250)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Mental Disorders [MESH:D001523] (2063)   Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Dementia [MESH:D003704] (471)   Frontotemporal Lobar Degeneration [MESH:D057174] (112)   Frontotemporal Dementia [MESH:D057180] (109)   Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Child Development Disorders, Pervasive [MESH:D002659] (157)   Autistic Disorder [MESH:D001321] (154)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Developmental Disabilities [MESH:D002658] (151)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12)  Intellectual Disability [MESH:D008607] (1109)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Oculodigitoesophagoduodenal syndrome [MESH:C537734] (58)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mental Retardation, Autosomal Recessive 1 [MESH:C565406] (19)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Mental Retardation, X-Linked, Syndromic, Turner Type [MESH:C567476] (18)  Mood Disorders [MESH:D019964] (257)   Affective Disorders, Psychotic [MESH:D000341] (248)   Bipolar Disorder [MESH:D001714] (247)   Major Affective Disorder 1 [MESH:C565111] (237)  Major Affective Disorder 7 [MESH:C567529] (136)  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) G. Phenomena and Processes  G. Phenomena and Processes  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)