Item 3 of 94 (back to results) previous next   methylmercuric chloride C004925               MeSH Unique Identifier: C004925 Chemical – Gene Interaction Note 1: Methylmercuric chloride binds to and affects the folding of ALB protein Note 2: Methylmercuric chloride results in increased expression of CD86 protein Click here for more information

Current search: C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140] > Bone Diseases [MESH:D001847] > Osteoarthropathy, Primary Hypertrophic [MESH:D010004] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Glutathione S-transferases [HGNC:GST] (460)   Glutathione S-transferases, soluble [HGNC:SGST] (447)   glutathione S-transferase mu 1 [HGNC:GSTM1] (144)  glutathione S-transferase pi 1 [HGNC:GSTP1] (218)  Homeoboxes [HGNC:homeobox] (219)   Homeoboxes, ANTP class [HGNC:HOXL] (152)   NKL subclass homeoboxes [HGNC:NKL] (109)   empty spiracles homeobox 2 [HGNC:EMX2] (7)  Nanog homeobox [HGNC:NANOG] (15)  Homeoboxes, POU class [HGNC:POU] (49)   POU class 5 homeobox 1 [HGNC:POU5F1] (22)  Homeoboxes, PRD class [HGNC:PRD] (60)   paired box 6 [HGNC:PAX6] (11)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 02 [HGNC:IL2] (144)  Paired boxes [HGNC:PAX] (37)   paired box 6 [HGNC:PAX6] (11) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  folding (77)  response to substance (623)  Decreases (5154)   expression (2187)  reaction (3393)  response to substance (713)  Increases (5571)   cleavage (666)  expression (3238)  glutathionylation (41) 4. Semantic Terms  4. Semantic Terms  Entity [STY:T071] (48056)   Physical Object [STY:T072] (47583)   Substance [STY:T167] (46174)   Chemical [STY:T103] (46110)   Chemical Viewed Functionally [STY:T120] (28747)   Indicator, Reagent, or Diagnostic Aid [STY:T130] (903)  Chemical Viewed Structurally [STY:T104] (44741)   Organic Chemical [STY:T109] (44144) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Breast [MESH:D001940] (56)   Limb-mammary syndrome [MESH:C535903] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Extremities [MESH:D005121] (484)   Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Head [MESH:D006257] (523)   Face [MESH:D005145] (387)   Coffin-Siris syndrome [MESH:C536436] (102)  Frontonasal dysplasia [MESH:C538065] (52)  Eye [MESH:D005123] (148)   Eyelids [MESH:D005143] (143)   Hay-Wells syndrome [MESH:C535847] (46)  Neck [MESH:D009333] (107)   Coffin-Siris syndrome [MESH:C536436] (102)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Upper Extremity [MESH:D001133] (240)   Arm Bones [MESH:D050280] (183)   Ulna [MESH:D014457] (96)   Ulnar-mammary syndrome [MESH:C536937] (57)  Skull [MESH:D012886] (610)   Facial Bones [MESH:D005147] (539)   Jaw [MESH:D007568] (524)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   Nephrons [MESH:D009399] (518)   Kidney Tubules [MESH:D007684] (510)   Kidney Tubules, Proximal [MESH:D007687] (504)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Nervous System [MESH:D009420] (587)   Peripheral Nervous System [MESH:D017933] (188)   Peripheral Nerves [MESH:D010525] (138)   Cranial Nerves [MESH:D003391] (96)   Optic Nerve [MESH:D009900] (70)   Coloboma of optic nerve [MESH:C535970] (43)  Sense Organs [MESH:D012679] (1060)   Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Peters anomaly [MESH:C537884] (465)  Eyelids [MESH:D005143] (146)   Hay-Wells syndrome [MESH:C535847] (46)  Stomatognathic System [MESH:D013284] (673)   Jaw [MESH:D007568] (528)   Mandible [MESH:D008334] (511)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Mouth [MESH:D009055] (194)   Dentition [MESH:D003817] (109)   Tooth [MESH:D014070] (61)   Incisor [MESH:D007180] (51)   Single upper central incisor [MESH:C537342] (50) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Helicobacter Infections [MESH:D016481] (579)  Pasteurellaceae Infections [MESH:D016871] (348)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Neisseriaceae Infections [MESH:D016870] (273)   Meningococcal Infections [MESH:D008589] (242)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Leprosy [MESH:D007918] (261)  Infection [MESH:D007239] (4109)   Intraabdominal Infections [MESH:D059413] (958)   Peritonitis [MESH:D010538] (800)  Sepsis [MESH:D018805] (3556)   Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)  Herpesviridae Infections [MESH:D006566] (1944)   Sarcoma, Kaposi [MESH:D012514] (1578)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  RNA Virus Infections [MESH:D012327] (4215)   Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Seropositivity [MESH:D006679] (480)  HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Seropositivity [MESH:D006679] (480)  HIV Wasting Syndrome [MESH:D019247] (1956)  Slow Virus Diseases [MESH:D012897] (782)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  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)  Protozoan Infections [MESH:D011528] (3014)   Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Visceral [MESH:D007898] (2149)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Dermoid Cyst [MESH:D003884] (34)   Ring dermoid of cornea [MESH:C535684] (29)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Tuberous Sclerosis [MESH:D014402] (635)  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 T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Megakaryoblastic, Acute [MESH:D007947] (279)  Lymphatic Vessel Tumors [MESH:D018190] (171)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, 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)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Rhabdoid Tumor [MESH:D018335] (61)   Rhabdoid Tumor Predisposition Syndrome 2 [MESH:C567643] (43)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Chondroma [MESH:D002812] (155)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Kaposi [MESH:D012514] (1578)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)   Rhabdomyosarcoma, Alveolar [MESH:D018232] (149)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Ependymoma [MESH:D004806] (76)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  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)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Teratoma [MESH:D013724] (51)   Dermoid Cyst [MESH:D003884] (34)   Ring dermoid of cornea [MESH:C535684] (29)  Trophoblastic Neoplasms [MESH:D014328] (68)   Gestational Trophoblastic Disease [MESH:D031901] (65)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Lewis Lung [MESH:D018827] (248)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Lobular [MESH:D018275] (305)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  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)   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, Lobular [MESH:D018275] (305)  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)   Ependymoma [MESH:D004806] (76)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  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)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Ependymoma [MESH:D004806] (76)  Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  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)  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)   Hemangioma [MESH:D006391] (690)  Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Sarcoma, Kaposi [MESH:D012514] (1578)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)  Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Liver Neoplasms [MESH:D008113] (6048)   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)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Testicular Neoplasms [MESH:D013736] (520)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Head and Neck Neoplasms [MESH:D006258] (4612)   Thyroid Neoplasms [MESH:D013964] (2040)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)  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)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Skin Neoplasms [MESH:D012878] (2992)   Sweat Gland Neoplasms [MESH:D013544] (46)  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)   Vaginal Neoplasms [MESH:D014625] (363)  Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Testicular Neoplasms [MESH:D013736] (520)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Carcinoma, Lewis Lung [MESH:D018827] (248)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Juvenile polyposis syndrome [MESH:C537702] (196)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Tuberous Sclerosis [MESH:D014402] (635)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Pregnancy Complications, Neoplastic [MESH:D011252] (71)   Trophoblastic Neoplasms [MESH:D014328] (67)   Gestational Trophoblastic Disease [MESH:D031901] (65)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Osteitis Deformans [MESH:D010001] (287)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Bone Diseases, Developmental [MESH:D001848] (3315)   Acromicric dysplasia [MESH:C535662] (520)  Marfan Syndrome [MESH:D008382] (646)  Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Dysostoses [MESH:D004413] (1019)   Rubinstein-Taybi Syndrome [MESH:D012415] (149)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Osteochondrodysplasias [MESH:D010009] (2440)   Spondyloenchondrodysplasia [MESH:C535782] (71)  Osteoglophonic dwarfism [MESH:C536050] (90)  Spondyloepimetaphyseal Dysplasia, Missouri Type [MESH:C566574] (142)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Camurati-Engelmann Syndrome [MESH:D003966] (492)  Enchondromatosis [MESH:D004687] (170)  Fibrous Dysplasia of Bone [MESH:D005357] (737)  Ellis-Van Creveld Syndrome [MESH:D004613] (50)   Asphyxiating Thoracic Dystrophy 3 [MESH:C567761] (15)  Short Rib-Polydactyly Syndrome [MESH:D012779] (17)   Short rib-polydactyly syndrome, Verma-Naumoff type [MESH:C537602] (15)  Bone Diseases, Endocrine [MESH:D001849] (747)   Acromegaly [MESH:D000172] (466)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)   Acro-Osteolysis [MESH:D030981] (548)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)   Intervertebral disc disease [MESH:C535531] (514)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Spinal Curvatures [MESH:D013121] (742)   Kyphosis [MESH:D007738] (637)  Scoliosis [MESH:D012600] (194)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Prognathism [MESH:D011378] (23)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Mandibular Diseases [MESH:D008336] (395)   Prognathism [MESH:D011378] (23)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Joint Diseases [MESH:D007592] (4657)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Arthrogryposis [MESH:D001176] (329)   Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Muscular Diseases [MESH:D009135] (4071)   Myopathy, Reducing Body, X-Linked, Childhood-Onset [MESH:C567468] (64)  Myopathy, Reducing Body, X-Linked, Early-Onset, Severe [MESH:C567469] (64)  Compartment Syndromes [MESH:D003161] (80)  Muscle Weakness [MESH:D018908] (478)  Arthrogryposis [MESH:D001176] (329)   Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169)   Myopathy, X-Linked, With Postural Muscle Atrophy [MESH:C567480] (64)  Scapuloperoneal Myopathy, X-Linked Dominant [MESH:C567481] (64)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Myositis [MESH:D009220] (2071)   Polymyositis [MESH:D017285] (2007)  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)   Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Craniofacial Abnormalities [MESH:D019465] (3098)   Craniofacial deafness hand syndrome [MESH:C536453] (27)  Frontonasal dysplasia [MESH:C538065] (52)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Costello Syndrome [MESH:D056685] (407)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Noonan Syndrome [MESH:D009634] (506)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Macrocephaly [MESH:D058627] (264)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Prognathism [MESH:D011378] (23)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Microcephaly [MESH:D008831] (700)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Limb-mammary syndrome [MESH:C535903] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Split-Hand/Foot Malformation 4 [MESH:C565344] (46)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Brachydactyly [MESH:D059327] (220)  Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Polydactyly [MESH:D017689] (318)   Short Rib-Polydactyly Syndrome [MESH:D012779] (17)   Short rib-polydactyly syndrome, Verma-Naumoff type [MESH:C537602] (15)  Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Abnormalities [MESH:D004065] (2127)   Hirschsprung Disease [MESH:D006627] (361)   Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease [MESH:C563789] (17)  Waardenburg Syndrome, Type 4c [MESH:C567679] (17)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Liver Neoplasms [MESH:D008113] (6048)   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)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Gastroenteritis [MESH:D005759] (4066)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43)  Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  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)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Megacolon [MESH:D008531] (386)   Hirschsprung Disease [MESH:D006627] (361)   Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease [MESH:C563789] (17)  Waardenburg Syndrome, Type 4c [MESH:C567679] (17)  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)   Inflammatory Bowel Disease 25, Autosomal Recessive [MESH:C567251] (43)  Inflammatory Bowel Disease 13 [MESH:C567384] (435)  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)   Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Intestinal Polyposis [MESH:D044483] (1610)   Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   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)   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)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Fatty Liver, Alcoholic [MESH:D005235] (657)  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, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  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)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Prognathism [MESH:D011378] (23)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Mandibular Diseases [MESH:D008336] (450)   Prognathism [MESH:D011378] (23)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  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)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Periodontal Diseases [MESH:D010510] (1001)   Periodontitis [MESH:D010518] (843)   Chronic Periodontitis [MESH:D055113] (231)  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)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Prognathism [MESH:D011378] (23)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Propping Zerres syndrome [MESH:C538052] (46)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Propping Zerres syndrome [MESH:C538052] (46) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Berylliosis [MESH:D001607] (2005)  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)   Berylliosis [MESH:D001607] (2005)  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)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Insufficiency [MESH:D012131] (841)   Asphyxiating Thoracic Dystrophy 3 [MESH:C567761] (15)  Hypoventilation [MESH:D007040] (360)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  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) 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)   Yemenite deaf-blind hypopigmentation syndrome [MESH:C536771] (17)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Craniofacial deafness hand syndrome [MESH:C536453] (27)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 35 [MESH:C563908] (17)  Deafness, Autosomal Recessive 67 [MESH:C565207] (16)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)  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)   Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  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)  Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)   Hypotension, Orthostatic [MESH:D007024] (679)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Focal cortical dysplasia of Taylor [MESH:C537067] (31)  Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)  Tourette Syndrome [MESH:D005879] (131)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease, Secondary [MESH:D010302] (327)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Brain Damage, Chronic [MESH:D001925] (311)   Cerebral Palsy [MESH:D002547] (300)   Cerebral Palsy, Spastic Quadriplegic, 1 [MESH:C567853] (99)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Homocystinuria [MESH:D006712] (93)   Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type [MESH:C565510] (20)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Brain Neoplasms [MESH:D001932] (2764)   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)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Vasospasm, Intracranial [MESH:D020301] (324)  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)  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)  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)  Huntington Disease [MESH:D006816] (540)  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)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Epilepsy [MESH:D004827] (6274)   Landau-Kleffner Syndrome [MESH:D018887] (87)  Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)  Myoclonic Epilepsy, Juvenile [MESH:D020190] (166)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Rolandic [MESH:D019305] (107)  Epilepsy, Frontal Lobe [MESH:D017034] (172)   Epilepsy, Nocturnal Frontal Lobe, Type 4 [MESH:C563679] (43)  Epilepsy, Generalized [MESH:D004829] (1431)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Spasms, Infantile [MESH:D013036] (468)  Seizures, Febrile [MESH:D003294] (229)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1250)   Acromegaly [MESH:D000172] (466)  Hyperprolactinemia [MESH:D006966] (603)  Leukoencephalopathies [MESH:D056784] (1916)   Ribose 5-Phosphate Isomerase Deficiency [MESH:C563212] (34)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis [MESH:D008581] (1506)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Prion Diseases [MESH:D017096] (488)   Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)  Dystonic Disorders [MESH:D020821] (729)   Myoclonic dystonia [MESH:C536096] (245)  Segawa syndrome, autosomal recessive [MESH:C537537] (220)  Juvenile-onset dystonia [MESH:C537704] (143)  Essential Tremor [MESH:D020329] (235)   Tremor hereditary essential, 1 [MESH:C536545] (97)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease, Secondary [MESH:D010302] (327)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Tic Disorders [MESH:D013981] (256)   Tourette Syndrome [MESH:D005879] (131)  Ocular Motility Disorders [MESH:D015835] (364)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Nerve Hypoplasia, Bilateral [MESH:C563492] (43)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  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)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  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)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Focal cortical dysplasia of Taylor [MESH:C537067] (31)  Neuronal Migration Disorders [MESH:D054081] (264)  Tuberous Sclerosis [MESH:D014402] (635)  Macrocephaly [MESH:D058627] (264)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Microcephaly [MESH:D008831] (700)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Neural Tube Defects [MESH:D009436] (2143)   Anencephaly [MESH:D000757] (120)   Neural tube defect, folate-sensitive [MESH:C536409] (111)  Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Nervous System Neoplasms [MESH:D009423] (3073)   Melanoma astrocytoma syndrome [MESH:C536149] (159)  Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Tuberous Sclerosis [MESH:D014402] (635)  von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Familial apoceruloplasmin deficiency [MESH:C536004] (211)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease [MESH:C563789] (17)  Alexander Disease [MESH:D038261] (168)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Huntington Disease [MESH:D006816] (540)  Tourette Syndrome [MESH:D005879] (131)  Tuberous Sclerosis [MESH:D014402] (635)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  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 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  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)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Parkinson Disease [MESH:D010300] (3595)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Prion Diseases [MESH:D017096] (475)   Scrapie [MESH:D012608] (462)  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 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)   Gait Disorders, Neurologic [MESH:D020233] (491)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  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)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Coffin-Siris syndrome [MESH:C536436] (102)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Down Syndrome [MESH:D004314] (1287)  Prader-Willi Syndrome [MESH:D011218] (46)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Pupil Disorders [MESH:D011681] (194)   Ectopia pupillae [MESH:C536185] (43)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Yemenite deaf-blind hypopigmentation syndrome [MESH:C536771] (17)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Craniofacial deafness hand syndrome [MESH:C536453] (27)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 35 [MESH:C563908] (17)  Deafness, Autosomal Recessive 67 [MESH:C565207] (16)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (501)   Blindness [MESH:D001766] (252)   Yemenite deaf-blind hypopigmentation syndrome [MESH:C536771] (17)  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 6, Autosomal Recessive [MESH:C567699] (54)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Diseases [MESH:D009135] (3538)   Myopathy, Reducing Body, X-Linked, Childhood-Onset [MESH:C567468] (64)  Myopathy, Reducing Body, X-Linked, Early-Onset, Severe [MESH:C567469] (64)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169)   Myopathy, X-Linked, With Postural Muscle Atrophy [MESH:C567480] (64)  Scapuloperoneal Myopathy, X-Linked Dominant [MESH:C567481] (64)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Myositis [MESH:D009220] (2069)   Polymyositis [MESH:D017285] (2007)  Myotonic Disorders [MESH:D020967] (138)   Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Myasthenic Syndromes, Congenital [MESH:D020294] (155)   Congenital myasthenic syndrome ib [MESH:C536089] (46)  Myasthenic syndrome, congenital, postsynaptic slow-channel [MESH:C536091] (73)  Myasthenic Syndrome, Congenital, Fast-Channel [MESH:C563832] (58)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Polyneuropathies [MESH:D011115] (1134)   Ribose 5-Phosphate Isomerase Deficiency [MESH:C563212] (34)  Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease [MESH:C563789] (17)  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 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  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)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Mercury Poisoning, Nervous System [MESH:D020262] (15)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Parasomnias [MESH:D020447] (453)   Sleep Arousal Disorders [MESH:D020921] (80)   Somnambulism [MESH:D013009] (75)   Epilepsy, Nocturnal Frontal Lobe, Type 4 [MESH:C563679] (43)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Conjunctival Diseases [MESH:D003229] (273)   Ring dermoid of cornea [MESH:C535684] (29)  Corneal Diseases [MESH:D003316] (1445)   Ring dermoid of cornea [MESH:C535684] (29)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Crystalline, of Schnyder [MESH:C535475] (22)  Corneal Opacity [MESH:D003318] (544)   Peters anomaly [MESH:C537884] (465)  Keratitis [MESH:D007634] (168)   Keratitis, hereditary [MESH:C537022] (43)  Eye Abnormalities [MESH:D005124] (1233)   Hay-Wells syndrome [MESH:C535847] (46)  Peters anomaly [MESH:C537884] (465)  Aniridia [MESH:D015783] (312)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Aniridia, type 2 [MESH:C536372] (43)  Coloboma [MESH:D003103] (315)   Coloboma of optic nerve [MESH:C535970] (43)  Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Aniridia [MESH:D015783] (312)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Aniridia, type 2 [MESH:C536372] (43)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Crystalline, of Schnyder [MESH:C535475] (22)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Lacrimal Duct Obstruction [MESH:D007767] (49)   Propping Zerres syndrome [MESH:C538052] (46)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Cataract, Autosomal Dominant [MESH:C565815] (58)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)  Ocular Motility Disorders [MESH:D015835] (1699)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Nerve Hypoplasia, Bilateral [MESH:C563492] (43)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Pupil Disorders [MESH:D011681] (230)   Ectopia pupillae [MESH:C536185] (43)  Refractive Errors [MESH:D012030] (457)   Myopia [MESH:D009216] (349)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinopathy of Prematurity [MESH:D012178] (353)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Uveal Diseases [MESH:D014603] (2428)   Iris Diseases [MESH:D007499] (348)   Aniridia [MESH:D015783] (312)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Aniridia, type 2 [MESH:C536372] (43)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784)  Vision Disorders [MESH:D014786] (534)   Blindness [MESH:D001766] (259)   Yemenite deaf-blind hypopigmentation syndrome [MESH:C536771] (17) 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)   Testicular Neoplasms [MESH:D013736] (520)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)  Penile Induration [MESH:D010411] (495)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Urogenital Abnormalities [MESH:D014564] (2065)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Hypospadias [MESH:D007021] (798)  Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Testicular Neoplasms [MESH:D013736] (520)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  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)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Renal hypouricemia [MESH:C537757] (71)  Fanconi Syndrome [MESH:D005198] (253)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Vesico-Ureteral Reflux [MESH:D014718] (58)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Uterine Diseases [MESH:D014591] (2479)   Uterine 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)  Vaginal Diseases [MESH:D014623] (446)   Vaginal Neoplasms [MESH:D014625] (363)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Abnormalities [MESH:D014564] (2043)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Vaginal Neoplasms [MESH:D014625] (363)  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)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  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)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Renal hypouricemia [MESH:C537757] (71)  Fanconi Syndrome [MESH:D005198] (253)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Vesico-Ureteral Reflux [MESH:D014718] (58)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Prenatal Injuries [MESH:D049188] (1314)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316)  Pregnancy Complications, Neoplastic [MESH:D011252] (71)   Trophoblastic Neoplasms [MESH:D014328] (67)   Gestational Trophoblastic Disease [MESH:D031901] (65) 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)  Coronary Vessel Anomalies [MESH:D003330] (317)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Noonan Syndrome [MESH:D009634] (506)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Vascular Malformations [MESH:D054079] (1098)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Cardiomyopathy, Dilated [MESH:D002311] (1576)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Endomyocardial Fibrosis [MESH:D004719] (521)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Coronary Vessel Anomalies [MESH:D003330] (317)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Noonan Syndrome [MESH:D009634] (506)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Angioedema [MESH:D000799] (837)  Compartment Syndromes [MESH:D003161] (80)  Hyperemia [MESH:D006940] (2372)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)  Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Abdominal [MESH:D017544] (1519)  Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Loeys-Dietz Syndrome [MESH:D055947] (263)  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 Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Vasospasm, Intracranial [MESH:D020301] (324)  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)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  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)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)  Thrombosis [MESH:D013927] (3101)   Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Malignant [MESH:D006974] (621)  Hypertension, Renal [MESH:D006977] (698)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Raynaud Disease [MESH:D011928] (490)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Anemia [MESH:D000740] (3966)   Anemia, Hemolytic [MESH:D000743] (3083)   Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to [MESH:C565545] (88)  Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to [MESH:C565557] (312)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, hypochromic microcytic [MESH:C536357] (164)  Anemia, Iron-Deficiency [MESH:D018798] (547)  Anemia, Macrocytic [MESH:D000748] (382)   Anemia, Megaloblastic [MESH:D000749] (288)   Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type [MESH:C565510] (20)  Blood Coagulation Disorders [MESH:D001778] (1828)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   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)   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)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemorrhagic Disorders [MESH:D006474] (3359)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  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)   Eosinophilia [MESH:D004802] (537)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Methemoglobinemia [MESH:D008708] (850)   NADH cytochrome B5 reductase deficiency [MESH:C537841] (66)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphatic Abnormalities [MESH:D044148] (251)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Sarcoidosis [MESH:D012507] (895)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  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 T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, 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)  Splenic Diseases [MESH:D013158] (1323)   Heterotaxy Syndrome [MESH:D059446] (84) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Drug-Induced [MESH:D000014] (1024)  Abnormalities, Multiple [MESH:D000015] (3192)   Coffin-Siris syndrome [MESH:C536436] (102)  Craniofacial deafness hand syndrome [MESH:C536453] (27)  Yemenite deaf-blind hypopigmentation syndrome [MESH:C536771] (17)  Ulnar-mammary syndrome [MESH:C536937] (57)  Multiple pterygium syndrome [MESH:C537377] (23)  Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141)  CHARGE Syndrome [MESH:D058747] (22)  Costello Syndrome [MESH:D056685] (407)  Down Syndrome [MESH:D004314] (1287)  Heterotaxy Syndrome [MESH:D059446] (84)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Marfan Syndrome [MESH:D008382] (646)  Prader-Willi Syndrome [MESH:D011218] (46)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Ectodermal Dysplasia [MESH:D004476] (938)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Ellis-Van Creveld Syndrome [MESH:D004613] (50)   Asphyxiating Thoracic Dystrophy 3 [MESH:C567761] (15)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Short Rib-Polydactyly Syndrome [MESH:D012779] (17)   Short rib-polydactyly syndrome, Verma-Naumoff type [MESH:C537602] (15)  Waardenburg Syndrome [MESH:D014849] (243)   Waardenburg syndrome type 2 [MESH:C536463] (55)  Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease [MESH:C563789] (17)  Waardenburg Syndrome, Type 4c [MESH:C567679] (17)  Abnormalities, Severe Teratoid [MESH:D009008] (124)   Anencephaly [MESH:D000757] (120)   Neural tube defect, folate-sensitive [MESH:C536409] (111)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Coronary Vessel Anomalies [MESH:D003330] (317)  Heterotaxy Syndrome [MESH:D059446] (84)  Marfan Syndrome [MESH:D008382] (646)  Noonan Syndrome [MESH:D009634] (506)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Vascular Malformations [MESH:D054079] (1108)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1018)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Prader-Willi Syndrome [MESH:D011218] (46)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Digestive System Abnormalities [MESH:D004065] (507)   Hirschsprung Disease [MESH:D006627] (361)   Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease [MESH:C563789] (17)  Waardenburg Syndrome, Type 4c [MESH:C567679] (17)  Eye Abnormalities [MESH:D005124] (1233)   Hay-Wells syndrome [MESH:C535847] (46)  Peters anomaly [MESH:C537884] (465)  Aniridia [MESH:D015783] (312)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Aniridia, type 2 [MESH:C536372] (43)  Coloboma [MESH:D003103] (315)   Coloboma of optic nerve [MESH:C535970] (43)  Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Lymphatic Abnormalities [MESH:D044148] (251)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Arthrogryposis [MESH:D001176] (329)   Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Craniofacial Abnormalities [MESH:D019465] (3064)   Craniofacial deafness hand syndrome [MESH:C536453] (27)  Frontonasal dysplasia [MESH:C538065] (52)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Noonan Syndrome [MESH:D009634] (506)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Macrocephaly [MESH:D058627] (264)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Prognathism [MESH:D011378] (23)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Microcephaly [MESH:D008831] (700)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Limb Deformities, Congenital [MESH:D017880] (1813)   Acromicric dysplasia [MESH:C535662] (520)  Limb-mammary syndrome [MESH:C535903] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Split-Hand/Foot Malformation 4 [MESH:C565344] (46)  Metaphyseal Anadysplasia 2 [MESH:C567771] (452)  Brachydactyly [MESH:D059327] (220)  Foot Deformities, Congenital [MESH:D005532] (538)   Jackson-Weiss syndrome [MESH:C537559] (149)  Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Polydactyly [MESH:D017689] (318)   Short Rib-Polydactyly Syndrome [MESH:D012779] (17)   Short rib-polydactyly syndrome, Verma-Naumoff type [MESH:C537602] (15)  Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Synostosis [MESH:D013580] (817)   Craniosynostoses [MESH:D003398] (438)   Jackson-Weiss syndrome [MESH:C537559] (149)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Acrocephalosyndactylia [MESH:D000168] (201)   Pfeiffer type acrocephalosyndactyly [MESH:C538582] (149)  Acrocephalopolysyndactyly Type II [MESH:C563187] (27)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Malformations of Cortical Development [MESH:D054220] (1406)   Focal cortical dysplasia of Taylor [MESH:C537067] (31)  Neuronal Migration Disorders [MESH:D054081] (264)  Tuberous Sclerosis [MESH:D014402] (635)  Macrocephaly [MESH:D058627] (264)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Microcephaly [MESH:D008831] (700)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Neural Tube Defects [MESH:D009436] (2143)   Anencephaly [MESH:D000757] (120)   Neural tube defect, folate-sensitive [MESH:C536409] (111)  Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Skin Abnormalities [MESH:D012868] (1723)   Multiple pterygium syndrome [MESH:C537377] (23)  Ectodermal Dysplasia [MESH:D004476] (958)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Ellis-Van Creveld Syndrome [MESH:D004613] (50)   Asphyxiating Thoracic Dystrophy 3 [MESH:C567761] (15)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Prognathism [MESH:D011378] (23)   Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism [MESH:C537686] (19)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Cleft Palate [MESH:D002972] (1330)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Propping Zerres syndrome [MESH:C538052] (46)  Urogenital Abnormalities [MESH:D014564] (2064)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Hypospadias [MESH:D007021] (798)  Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Camurati-Engelmann Syndrome [MESH:D003966] (492)  CHARGE Syndrome [MESH:D058747] (22)  Costello Syndrome [MESH:D056685] (407)  Cystic Fibrosis [MESH:D003550] (760)  Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478)  Kallmann Syndrome [MESH:D017436] (147)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Marfan Syndrome [MESH:D008382] (646)  Osteoarthropathy, Primary Hypertrophic [MESH:D010004] (94)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   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)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Prader-Willi Syndrome [MESH:D011218] (46)  Rubinstein-Taybi Syndrome [MESH:D012415] (149)  22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Aniridia [MESH:D015783] (312)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Aniridia, type 2 [MESH:C536372] (43)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Corneal Dystrophy, Crystalline, of Schnyder [MESH:C535475] (22)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Myopathy, Reducing Body, X-Linked, Childhood-Onset [MESH:C567468] (64)  Myopathy, Reducing Body, X-Linked, Early-Onset, Severe [MESH:C567469] (64)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169)   Myopathy, X-Linked, With Postural Muscle Atrophy [MESH:C567480] (64)  Scapuloperoneal Myopathy, X-Linked Dominant [MESH:C567481] (64)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease [MESH:C563789] (17)  Alexander Disease [MESH:D038261] (168)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Huntington Disease [MESH:D006816] (540)  Tourette Syndrome [MESH:D005879] (131)  Tuberous Sclerosis [MESH:D014402] (635)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  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 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia type 5A, recessive [MESH:C536871] (79)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  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)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutamine deficiency, congenital [MESH:C536832] (117)  Glutathione synthetase deficiency [MESH:C536835] (88)  Hyperhomocysteinemia [MESH:D020138] (1724)   Homocystinuria [MESH:D006712] (93)   Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type [MESH:C565510] (20)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Homocystinuria [MESH:D006712] (93)   Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type [MESH:C565510] (20)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Transaldolase Deficiency [MESH:C563207] (61)  Ribose 5-Phosphate Isomerase Deficiency [MESH:C563212] (34)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Adrenoleukodystrophy [MESH:D000326] (1348)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Renal hypouricemia [MESH:C537757] (71)  Fanconi Syndrome [MESH:D005198] (253)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Muscular Dystrophy, Emery-Dreifuss [MESH:D020389] (169)   Myopathy, X-Linked, With Postural Muscle Atrophy [MESH:C567480] (64)  Scapuloperoneal Myopathy, X-Linked Dominant [MESH:C567481] (64)  Myotonic Dystrophy [MESH:D009223] (48)   Dystrophia myotonica 1 [MESH:C538008] (25)  Myasthenic Syndromes, Congenital [MESH:D020294] (155)   Congenital myasthenic syndrome ib [MESH:C536089] (46)  Myasthenic syndrome, congenital, postsynaptic slow-channel [MESH:C536091] (73)  Myasthenic Syndrome, Congenital, Fast-Channel [MESH:C563832] (58)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Juvenile polyposis syndrome [MESH:C537702] (196)  Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Tuberous Sclerosis [MESH:D014402] (635)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Colorectal Adenomatous Polyposis, Autosomal Recessive [MESH:C563924] (28)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)  Cutis Laxa [MESH:D003483] (177)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Ectodermal Dysplasia [MESH:D004476] (958)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Ellis-Van Creveld Syndrome [MESH:D004613] (50)   Asphyxiating Thoracic Dystrophy 3 [MESH:C567761] (15)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Cystic Fibrosis [MESH:D003550] (760)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Jaundice, Neonatal [MESH:D007567] (290)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Infant, Premature, Diseases [MESH:D007235] (1292)   Retinopathy of Prematurity [MESH:D012178] (353)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Immune dysfunction with T-cell inactivation due to calcium entry defect 2 [MESH:C557827] (20) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Marfan Syndrome [MESH:D008382] (646)  Noonan Syndrome [MESH:D009634] (506)  Penile Induration [MESH:D010411] (495)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Cutis Laxa [MESH:D003483] (177)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Homocystinuria [MESH:D006712] (93)   Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type [MESH:C565510] (20)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Keratosis [MESH:D007642] (1941)  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)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Eczema [MESH:D004485] (235)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Drug Eruptions [MESH:D003875] (2697)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Pigmentation Disorders [MESH:D010859] (1215)   Propping Zerres syndrome [MESH:C538052] (46)  Hypopigmentation [MESH:D017496] (718)   Yemenite deaf-blind hypopigmentation syndrome [MESH:C536771] (17)  Skin Abnormalities [MESH:D012868] (1709)   Multiple pterygium syndrome [MESH:C537377] (23)  Ectodermal Dysplasia [MESH:D004476] (958)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Ellis-Van Creveld Syndrome [MESH:D004613] (50)   Asphyxiating Thoracic Dystrophy 3 [MESH:C567761] (15)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Eczema [MESH:D004485] (235)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Dermatitis, Atopic [MESH:D003876] (2052)  Cutis Laxa [MESH:D003483] (177)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Ectodermal Dysplasia [MESH:D004476] (958)   Rapp-Hodgkin syndrome [MESH:C535289] (46)  Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Hay-Wells syndrome [MESH:C535847] (46)  Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)  Propping Zerres syndrome [MESH:C538052] (46)  Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)  Ellis-Van Creveld Syndrome [MESH:D004613] (50)   Asphyxiating Thoracic Dystrophy 3 [MESH:C567761] (15)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Skin Neoplasms [MESH:D012878] (2991)   Sweat Gland Neoplasms [MESH:D013544] (46)  Sweat Gland Diseases [MESH:D013543] (231)   Sweat Gland Neoplasms [MESH:D013544] (46) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Metabolic Syndrome X [MESH:D024821] (2151)  Acid-Base Imbalance [MESH:D000137] (854)   Alkalosis [MESH:D000471] (384)  Acidosis [MESH:D000138] (626)   Acidosis, Lactic [MESH:D000140] (204)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Homocystinuria [MESH:D006712] (93)   Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type [MESH:C565510] (20)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Hypercalcemia [MESH:D006934] (1999)  Hypocalcemia [MESH:D006996] (378)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Li-Fraumeni Syndrome [MESH:D016864] (859)  Severe Combined Immunodeficiency [MESH:D016511] (294)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Immune dysfunction with T-cell inactivation due to calcium entry defect 2 [MESH:C557827] (20)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Hypoglycemia [MESH:D007003] (2420)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Iron Metabolism Disorders [MESH:D019189] (2139)   Familial apoceruloplasmin deficiency [MESH:C536004] (211)  Anemia, Iron-Deficiency [MESH:D018798] (547)  Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipid Metabolism, Inborn Errors [MESH:D008052] (461)  Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipoproteinemias [MESH:D006951] (903)   Hypercholesterolemia, Autosomal Dominant, 3 [MESH:C566337] (49)  Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutamine deficiency, congenital [MESH:C536832] (117)  Glutathione synthetase deficiency [MESH:C536835] (88)  Hyperhomocysteinemia [MESH:D020138] (1724)   Homocystinuria [MESH:D006712] (93)   Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type [MESH:C565510] (20)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Alexander Disease [MESH:D038261] (168)  Homocystinuria [MESH:D006712] (93)   Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type [MESH:C565510] (20)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Transaldolase Deficiency [MESH:C563207] (61)  Ribose 5-Phosphate Isomerase Deficiency [MESH:C563212] (34)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sialic Acid Storage Disease [MESH:D029461] (63)  Sphingolipidoses [MESH:D013106] (582)   Gaucher Disease [MESH:D005776] (299)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Adrenoleukodystrophy [MESH:D000326] (1348)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Renal hypouricemia [MESH:C537757] (71)  Fanconi Syndrome [MESH:D005198] (253)  Mitochondrial Diseases [MESH:D028361] (2561)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Pyruvate Dehydrogenase Complex Deficiency Disease [MESH:D015325] (149)   Pyruvate Dehydrogenase E3-Binding Protein Deficiency [MESH:C565447] (25)  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 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)   Lipodystrophy [MESH:D008060] (930)   Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hypocalcemia [MESH:D006996] (368)  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)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Prader-Willi Syndrome [MESH:D011218] (46)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Adrenal Cortex Diseases [MESH:D000303] (969)   Pigmented Nodular Adrenocortical Disease, Primary, 2 [MESH:C566472] (21)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   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 Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Ovarian Neoplasms [MESH:D010051] (3275)  Pituitary Neoplasms [MESH:D010911] (981)  Testicular Neoplasms [MESH:D013736] (520)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   Melanoma-Pancreatic Cancer Syndrome [MESH:C563985] (159)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Delayed [MESH:D011628] (449)  Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Kallmann Syndrome [MESH:D017436] (147)  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)   Testicular Neoplasms [MESH:D013736] (520)  Cryptorchidism [MESH:D003456] (215)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Hypoparathyroidism [MESH:D007011] (376)   22q11 Deletion Syndrome [MESH:D058165] (237)   DiGeorge Syndrome [MESH:D004062] (236)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Hyperprolactinemia [MESH:D006966] (603)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Thyroid Neoplasms [MESH:D013964] (2040)  Hyperthyroxinemia [MESH:D006981] (659)   Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Spondyloenchondrodysplasia [MESH:C535782] (71)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  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)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  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)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Immune Complex Diseases [MESH:D007105] (782)   Serum Sickness [MESH:D012713] (484)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Complement Component 7 Deficiency [MESH:C566443] (37)  Complement Component 6 Deficiency [MESH:C567307] (35)  Agammaglobulinemia [MESH:D000361] (156)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Seropositivity [MESH:D006679] (480)  HIV Wasting Syndrome [MESH:D019247] (1956)  Severe Combined Immunodeficiency [MESH:D016511] (315)   Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)  Immune dysfunction with T-cell inactivation due to calcium entry defect 2 [MESH:C557827] (20)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  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 T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, 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)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Plaque, Atherosclerotic [MESH:D058226] (696)  Ventricular Remodeling [MESH:D020257] (686)  Alopecia [MESH:D000505] (1383)   Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis [MESH:C567770] (35)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Urinary Calculi [MESH:D014545] (521)   Renal hypouricemia [MESH:C537757] (71)  Cysts [MESH:D003560] (133)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  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)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Nails, Malformed [MESH:D009264] (184)   Propping Zerres syndrome [MESH:C538052] (46)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Emphysema [MESH:D004646] (1096)  Gliosis [MESH:D005911] (1419)  Hyperammonemia [MESH:D022124] (322)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Muscle Weakness [MESH:D018908] (478)  Necrosis [MESH:D009336] (4019)  Neointima [MESH:D058426] (814)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Tachycardia [MESH:D013610] (3339)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Translocation, Genetic [MESH:D014178] (557)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)  Recurrence [MESH:D012008] (830)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Fibrosis [MESH:D005355] (3133)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Peritoneal Fibrosis [MESH:D056627] (488)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  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)   Hematoma [MESH:D006406] (281)  Shock, Hemorrhagic [MESH:D012771] (2042)  Gastrointestinal Hemorrhage [MESH:D006471] (815)   Peptic Ulcer Hemorrhage [MESH:D010438] (553)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Inflammation [MESH:D007249] (5241)   Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Intraoperative Complications [MESH:D007431] (131)   Malignant Hyperthermia [MESH:D008305] (92)   Multiple pterygium syndrome [MESH:C537377] (23)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Neoplasm, Residual [MESH:D018365] (478)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Postoperative Complications [MESH:D011183] (5311)   Pain, Postoperative [MESH:D010149] (529)  Malignant Hyperthermia [MESH:D008305] (92)   Multiple pterygium syndrome [MESH:C537377] (23)  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)  Signs and Symptoms [MESH:D012816] (10659)   Asthenia [MESH:D001247] (376)  Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Neurologic Manifestations [MESH:D009461] (8702)   Gait Disorders, Neurologic [MESH:D020233] (491)  Seizures [MESH:D012640] (4502)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (984)   Cerebellar Ataxia [MESH:D002524] (289)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  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)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Coffin-Siris syndrome [MESH:C536436] (102)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Gaze Palsy, Familial Horizontal, with Progressive Scoliosis [MESH:C564593] (8)  Supranuclear Palsy, Progressive [MESH:D013494] (235)   Progressive supranuclear palsy atypical [MESH:C537240] (142)  Pupil Disorders [MESH:D011681] (194)   Ectopia pupillae [MESH:C536185] (43)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)   Yemenite deaf-blind hypopigmentation syndrome [MESH:C536771] (17)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Craniofacial deafness hand syndrome [MESH:C536453] (27)  Deafness, Autosomal Dominant 9 [MESH:C563335] (33)  Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Deafness, Autosomal Recessive 35 [MESH:C563908] (17)  Deafness, Autosomal Recessive 67 [MESH:C565207] (16)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (444)   Blindness [MESH:D001766] (178)   Yemenite deaf-blind hypopigmentation syndrome [MESH:C536771] (17)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Pain, Postoperative [MESH:D010149] (529)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Hyperphagia [MESH:D006963] (206)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Respiratory Sounds [MESH:D012135] (713)  Hypoventilation [MESH:D007040] (359)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005) 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)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Lead Poisoning [MESH:D007855] (515)  Manganese Poisoning [MESH:D020149] (2214)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Mercury Poisoning [MESH:D008630] (193)   Mercury Poisoning, Nervous System [MESH:D020262] (15)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Drug Overdose [MESH:D062787] (513)  Marijuana Abuse [MESH:D002189] (1132)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Tobacco Use Disorder [MESH:D014029] (628)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Cardiomyopathy, Alcoholic [MESH:D002310] (354)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950)  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)  Heat Stress Disorders [MESH:D018882] (226)  Spinal Cord Injuries [MESH:D013119] (2688)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Organometallic Compounds [MESH:D009942] (4369)   Organomercury Compounds [MESH:D009941] (134)   Alkylmercury Compounds [MESH:D000479] (45)   Methylmercury Compounds [MESH:D008767] (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)   Physical Examination [MESH:D010808] (1041)   Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51) 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)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Coffin-Siris syndrome [MESH:C536436] (102)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  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)  Lewy Body Disease [MESH:D020961] (139)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Aniridia cerebellar ataxia mental deficiency [MESH:C536370] (43)  Coffin-Siris syndrome [MESH:C536436] (102)  Growth mental deficiency syndrome of Myhre [MESH:C537620] (51)  Cerebrooculofacioskeletal Syndrome 4 [MESH:C565184] (75)  Sleep Disorders [MESH:D012893] (148)   Parasomnias [MESH:D020447] (57)   Sleep Arousal Disorders [MESH:D020921] (46)   Somnambulism [MESH:D013009] (44)   Epilepsy, Nocturnal Frontal Lobe, Type 4 [MESH:C563679] (43)