Item 15 of 52 (back to results) previous next   tesaglitazar C501413               MeSH Unique Identifier: C501413 Chemical – Gene Interaction Note 1: [tesaglitazar results in increased activity of PPARA protein] which results in increased expression of FABP1 protein Note 2: Tesaglitazar results in increased expression of FABP1 protein Click here for more information

Current search: C18. Nutritional and Metabolic Diseases: Metabolic Diseases [MESH:D008659] > Mitochondrial Diseases [MESH:D028361] > Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Fatty acid binding protein family [HGNC:FABP] (151)   fatty acid binding protein 1, liver [HGNC:FABP1] (56)  Nuclear hormone receptors [HGNC:NR] (1322)   peroxisome proliferator-activated receptor alpha [HGNC:PPARA] (156)  peroxisome proliferator-activated receptor gamma [HGNC:PPARG] (234) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  Increases (5571)   activity (2865)  expression (3238) A. Anatomy  A. Anatomy  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) 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)  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)   Staphylococcal Infections [MESH:D013203] (264)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Paratuberculosis [MESH:D010283] (427)  Tuberculosis [MESH:D014376] (992)   Tuberculosis, Pulmonary [MESH:D014397] (678)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  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)   Herpesviridae Infections [MESH:D006566] (1944)   Sarcoma, Kaposi [MESH:D012514] (1578)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  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)  Picornaviridae Infections [MESH:D010850] (1672)   Enterovirus Infections [MESH:D004769] (241)   Coxsackievirus Infections [MESH:D003384] (194)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   HIV Wasting Syndrome [MESH:D019247] (1956)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Leishmaniasis, Visceral [MESH:D007898] (2149)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Hamartoma [MESH:D006222] (1484)  Neoplasms, Radiation-Induced [MESH:D009381] (174)  Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Leukemia, Erythroblastic, Acute [MESH:D004915] (89)  Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphatic Vessel Tumors [MESH:D018190] (171)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, T-Cell [MESH:D016399] (1405)  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)   Mixed Tumor, Mullerian [MESH:D018200] (64)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibrosarcoma [MESH:D005354] (90)  Solitary Fibrous Tumors [MESH:D054364] (79)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Smooth Muscle Tumor [MESH:D018235] (132)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Fibrosarcoma [MESH:D005354] (90)  Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Kaposi [MESH:D012514] (1578)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   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)   Melanoma [MESH:D008545] (3508)  Carcinoma, Neuroendocrine [MESH:D018278] (262)   Carcinoma, Medullary [MESH:D018276] (181)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Neurilemmoma [MESH:D009442] (36)   Schwannomatosis [MESH:C536641] (29)  Neuroma, Acoustic [MESH:D009464] (30)   Neurofibromatosis 2 [MESH:D016518] (29)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Squamous Cell [MESH:D002294] (4294)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   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)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma, Neuroendocrine [MESH:D018278] (262)   Carcinoma, Medullary [MESH:D018276] (181)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Lobular [MESH:D018275] (305)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma, Medullary [MESH:D018276] (181)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   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)   Carcinoma, Squamous Cell [MESH:D002294] (4294)  Papilloma [MESH:D010212] (2243)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Nerve Sheath Neoplasms [MESH:D018317] (365)   Neurofibroma [MESH:D009455] (177)   Neurofibromatoses [MESH:D017253] (146)   Schwannomatosis [MESH:C536641] (29)  Neurofibromatosis 2 [MESH:D016518] (29)  Neuroma [MESH:D009463] (37)   Neurilemmoma [MESH:D009442] (36)   Schwannomatosis [MESH:C536641] (29)  Neuroma, Acoustic [MESH:D009464] (30)   Neurofibromatosis 2 [MESH:D016518] (29)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   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)   Melanoma [MESH:D008545] (3508)  Carcinoma, Neuroendocrine [MESH:D018278] (184)   Carcinoma, Medullary [MESH:D018276] (181)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Neurilemmoma [MESH:D009442] (35)   Schwannomatosis [MESH:C536641] (29)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Sarcoma, Kaposi [MESH:D012514] (1578)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioma, capillary infantile [MESH:C535860] (190)  Hemangioblastoma [MESH:D018325] (395)  Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Gastrointestinal Neoplasms [MESH:D005770] (6452)   Esophageal Neoplasms [MESH:D004938] (3737)  Stomach Neoplasms [MESH:D013274] (4942)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Neoplasms [MESH:D013964] (2040)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Head and Neck Neoplasms [MESH:D006258] (4612)   Esophageal Neoplasms [MESH:D004938] (3737)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Laryngeal Neoplasms [MESH:D007822] (68)  Pharyngeal Neoplasms [MESH:D010610] (1520)  Thyroid Neoplasms [MESH:D013964] (2040)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Skin Neoplasms [MESH:D012878] (2992)   Schwannomatosis [MESH:C536641] (29)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   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)  Wilms Tumor [MESH:D009396] (553)  Neoplasms, Experimental [MESH:D009374] (5218)   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)   Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Meningioma, familial [MESH:C537443] (195)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Wilms Tumor [MESH:D009396] (553)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Neurofibromatoses [MESH:D017253] (146)   Schwannomatosis [MESH:C536641] (29)  Neurofibromatosis 2 [MESH:D016518] (29)  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 Diseases, Developmental [MESH:D001848] (3315)   Dwarfism [MESH:D004392] (778)   Congenital Hypothyroidism [MESH:D003409] (266)   Thyroid Dyshormonogenesis 2A [MESH:C563206] (52)  Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Syndactyly [MESH:D013576] (487)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Gigantism [MESH:D005877] (46)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Osteochondrodysplasias [MESH:D010009] (2440)   Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Bone Diseases, Endocrine [MESH:D001849] (747)   Congenital Hypothyroidism [MESH:D003409] (266)   Thyroid Dyshormonogenesis 2A [MESH:C563206] (52)  Gigantism [MESH:D005877] (46)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Bone Resorption [MESH:D001862] (2352)   Alveolar Bone Loss [MESH:D016301] (220)  Spinal Diseases [MESH:D013122] (2485)   Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Cartilage Diseases [MESH:D002357] (438)   Keutel syndrome [MESH:C536167] (102)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Joint Diseases [MESH:D007592] (4657)   Arthrogryposis [MESH:D001176] (329)  Ankylosis [MESH:D000844] (479)   Spondylitis, Ankylosing [MESH:D013167] (431)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Synovitis [MESH:D013585] (270)   Synovitis granulomatous with uveitis and cranial neuropathies [MESH:C538157] (16)  Muscular Diseases [MESH:D009135] (4071)   VLCAD deficiency [MESH:C536353] (55)  Systemic carnitine deficiency [MESH:C536778] (92)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Arthrogryposis [MESH:D001176] (329)  Muscle Rigidity [MESH:D009127] (617)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Arthrogryposis [MESH:D001176] (329)  Craniofacial Abnormalities [MESH:D019465] (3098)   Loeys-Dietz Syndrome [MESH:D055947] (263)  Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Microcephaly [MESH:D008831] (700)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Limb Deformities, Congenital [MESH:D017880] (1813)   Syndactyly [MESH:D013576] (487)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Syndactyly [MESH:D013576] (487)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  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)   Biliary Atresia [MESH:D001656] (68)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Cholangitis [MESH:D002761] (203)   Cholangitis, Sclerosing [MESH:D015209] (93)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Common Bile Duct Diseases [MESH:D003137] (47)   Choledocholithiasis [MESH:D042883] (26)  Cholelithiasis [MESH:D002769] (373)   Choledocholithiasis [MESH:D042883] (26)  Gallstones [MESH:D042882] (350)  Gallbladder Diseases [MESH:D005705] (1215)   Cholecystolithiasis [MESH:D041761] (353)   Gallstones [MESH:D042882] (350)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Biliary Atresia [MESH:D001656] (68)  Digestive System Neoplasms [MESH:D004067] (7493)   Gastrointestinal Neoplasms [MESH:D005770] (6460)   Esophageal Neoplasms [MESH:D004938] (3737)  Stomach Neoplasms [MESH:D013274] (4942)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Neoplasms [MESH:D004938] (3737)  Deglutition Disorders [MESH:D003680] (1538)   Esophageal Motility Disorders [MESH:D015154] (1489)   Gastroesophageal Reflux [MESH:D005764] (1465)  Gastroenteritis [MESH:D005759] (4066)   Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Esophageal Neoplasms [MESH:D004938] (3737)  Stomach Neoplasms [MESH:D013274] (4942)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Sitosterolemia [MESH:C537345] (82)  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)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)   Duodenal Ulcer [MESH:D004381] (1549)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Malabsorption Syndromes [MESH:D008286] (492)   Glucose-Galactose Malabsorption [MESH:C562602] (49)  Celiac Disease [MESH:D002446] (340)  Steatorrhea [MESH:D045602] (41)   Bile Acid Malabsorption, Primary [MESH:C567652] (38)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48)  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)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Glycogen Storage Disease 0, Liver [MESH:C565485] (45)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Budd-Chiari Syndrome [MESH:D006502] (164)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Zellweger Syndrome [MESH:D015211] (182)  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)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  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)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Pancreatic Diseases [MESH:D010182] (4453)   Congenital Hyperinsulinism [MESH:D044903] (132)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Periodontal Diseases [MESH:D010510] (1001)   Periodontal Atrophy [MESH:D055093] (225)   Alveolar Bone Loss [MESH:D016301] (220)  Periodontitis [MESH:D010518] (843)   Chronic Periodontitis [MESH:D055113] (231)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  Pharyngeal Diseases [MESH:D010608] (1562)   Pharyngeal Neoplasms [MESH:D010610] (1520)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Respiratory System Abnormalities [MESH:D015619] (243)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Laryngeal Diseases [MESH:D007818] (215)   Laryngeal Neoplasms [MESH:D007822] (68)  Lung Diseases [MESH:D008171] (7249)   Pulmonary Alveolar Microlithiasis [MESH:C562405] (44)  Hypertension, Pulmonary [MESH:D006976] (2000)  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)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Lung Neoplasms [MESH:D008175] (6012)   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)   Nasal Obstruction [MESH:D015508] (132)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Insufficiency [MESH:D012131] (841)   Airway Obstruction [MESH:D000402] (191)   Nasal Obstruction [MESH:D015508] (132)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Tuberculosis, Pulmonary [MESH:D014397] (678)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Laryngeal Neoplasms [MESH:D007822] (68)  Lung Neoplasms [MESH:D008175] (6013)   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)   Deaf-Blind Disorders [MESH:D054062] (132)   Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Donnai-Barrow syndrome [MESH:C536390] (40)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 2B [MESH:C567214] (18)  Deafness, Autosomal Dominant 2A [MESH:C567441] (36)  Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Retrocochlear Diseases [MESH:D012181] (241)   Vestibulocochlear Nerve Diseases [MESH:D000160] (45)   Neuroma, Acoustic [MESH:D009464] (30)   Neurofibromatosis 2 [MESH:D016518] (29)  Laryngeal Diseases [MESH:D007818] (211)   Laryngeal Neoplasms [MESH:D007822] (68)  Nose Diseases [MESH:D009668] (1504)   Nasal Obstruction [MESH:D015508] (132)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Laryngeal Neoplasms [MESH:D007822] (68)  Pharyngeal Neoplasms [MESH:D010610] (1520)  Neuroma, Acoustic [MESH:D009464] (30)   Neurofibromatosis 2 [MESH:D016518] (29)  Pharyngeal Diseases [MESH:D010608] (1605)   Pharyngeal Neoplasms [MESH:D010610] (1520) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Chronobiology Disorders [MESH:D021081] (970)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  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)   Multiple System Atrophy [MESH:D019578] (102)   Shy-Drager Syndrome [MESH:D012791] (99)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Brain Neoplasms [MESH:D001932] (2764)  Basal Ganglia Diseases [MESH:D001480] (4268)   Multiple System Atrophy [MESH:D019578] (158)   Shy-Drager Syndrome [MESH:D012791] (99)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Galactosemias [MESH:D005693] (69)  Homocystinuria [MESH:D006712] (93)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Phenylketonurias [MESH:D010661] (156)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Peroxisomal Disorders [MESH:D018901] (1472)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Dysequilibrium syndrome [MESH:C535731] (83)  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)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  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)  Lewy Body Disease [MESH:D020961] (1143)  Epilepsy [MESH:D004827] (6274)   Amish Infantile Epilepsy Syndrome [MESH:C563799] (46)  Seizures, Febrile [MESH:D003294] (229)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Frontal Lobe [MESH:D017034] (172)   Epilepsy, Nocturnal Frontal Lobe, Type 4 [MESH:C563679] (43)  Epilepsy, Generalized [MESH:D004829] (1431)   Spasms, Infantile [MESH:D013036] (468)  Seizures [MESH:D012640] (4502)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)   Migraine without Aura [MESH:D020326] (408)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Hypopituitarism [MESH:D007018] (732)  Inappropriate ADH Syndrome [MESH:D007177] (178)  Hyperpituitarism [MESH:D006964] (1250)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  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)  Movement Disorders [MESH:D009069] (4823)   Dystonic Disorders [MESH:D020821] (729)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Multiple System Atrophy [MESH:D019578] (158)   Shy-Drager Syndrome [MESH:D012791] (99)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Cranial Nerve Diseases [MESH:D003389] (2004)   Synovitis granulomatous with uveitis and cranial neuropathies [MESH:C538157] (16)  Cranial Nerve Neoplasms [MESH:D003390] (36)   Neuroma, Acoustic [MESH:D009464] (30)   Neurofibromatosis 2 [MESH:D016518] (29)  Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Vestibulocochlear Nerve Diseases [MESH:D000160] (111)   Neuroma, Acoustic [MESH:D009464] (30)   Neurofibromatosis 2 [MESH:D016518] (29)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Multiple Sclerosis [MESH:D009103] (1716)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  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)   Donnai-Barrow syndrome [MESH:C536390] (40)  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)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neurocutaneous Syndromes [MESH:D020752] (1230)   von Hippel-Lindau Disease [MESH:D006623] (580)  Neurofibromatoses [MESH:D017253] (146)   Schwannomatosis [MESH:C536641] (29)  Neurofibromatosis 2 [MESH:D016518] (29)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Shy-Drager Syndrome [MESH:D012791] (99)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Neurofibromatoses [MESH:D017253] (146)   Schwannomatosis [MESH:C536641] (29)  Neurofibromatosis 2 [MESH:D016518] (29)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Multiple System Atrophy [MESH:D019578] (158)   Shy-Drager Syndrome [MESH:D012791] (99)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Neurologic Manifestations [MESH:D009461] (8964)   Reflex, Abnormal [MESH:D012021] (485)  Dyskinesias [MESH:D020820] (3365)   Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Dysequilibrium syndrome [MESH:C535731] (83)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Dysequilibrium syndrome [MESH:C535731] (83)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Histidinemia [MESH:C538320] (87)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Allan-Herndon-Dudley syndrome [MESH:C537047] (24)  Mental Retardation, X-Linked 30 [MESH:C563146] (40)  Mental Retardation, X-Linked 91 [MESH:C564482] (7)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Muscle Hypotonia [MESH:D009123] (258)   Allan-Herndon-Dudley syndrome [MESH:C537047] (24)  Muscular Atrophy [MESH:D009133] (1234)   Allan-Herndon-Dudley syndrome [MESH:C537047] (24)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Seizures [MESH:D012640] (4514)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)   Deaf-Blind Disorders [MESH:D054062] (132)   Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Donnai-Barrow syndrome [MESH:C536390] (40)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 2B [MESH:C567214] (18)  Deafness, Autosomal Dominant 2A [MESH:C567441] (36)  Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (501)   Blindness [MESH:D001766] (252)   Deaf-Blind Disorders [MESH:D054062] (132)   Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Muscular Diseases [MESH:D009135] (3538)   VLCAD deficiency [MESH:C536353] (55)  Systemic carnitine deficiency [MESH:C536778] (92)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenic Syndromes, Congenital [MESH:D020294] (155)   Endplate Acetylcholinesterase Deficiency [MESH:C566415] (16)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Mononeuropathies [MESH:D020422] (604)   Sciatic Neuropathy [MESH:D020426] (477)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  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)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)  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)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eye Abnormalities [MESH:D005124] (1233)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Corneal Opacity [MESH:D003318] (544)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Cone-Rod Dystrophy 10 [MESH:C564597] (30)  Retinitis Pigmentosa 35 [MESH:C565206] (30)  Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Refractive Errors [MESH:D012030] (457)   Myopia [MESH:D009216] (349)   Donnai-Barrow syndrome [MESH:C536390] (40)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Stargardt disease 4 [MESH:C535521] (63)  Macular Edema [MESH:D008269] (557)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Cone-Rod Dystrophy 10 [MESH:C564597] (30)  Retinitis Pigmentosa 35 [MESH:C565206] (30)  Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  Uveitis [MESH:D014605] (2157)   Synovitis granulomatous with uveitis and cranial neuropathies [MESH:C538157] (16)  Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784)  Vision Disorders [MESH:D014786] (534)   Blindness [MESH:D001766] (259)   Deaf-Blind Disorders [MESH:D054062] (132)   Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Testicular Diseases [MESH:D013733] (451)   Testicular Microlithiasis [MESH:C566478] (44)  Cryptorchidism [MESH:D003456] (215)  Urogenital Abnormalities [MESH:D014564] (2065)   Cryptorchidism [MESH:D003456] (215)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   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)  Wilms Tumor [MESH:D009396] (553)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Zellweger Syndrome [MESH:D015211] (182)  Diabetes Insipidus [MESH:D003919] (354)   Diabetes Insipidus, Neurogenic [MESH:D020790] (100)  Hyperoxaluria [MESH:D006959] (1498)   Hyperoxaluria, Primary [MESH:D006960] (63)   Primary hyperoxaluria type 1 [MESH:C536414] (48)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Donnai-Barrow syndrome [MESH:C536390] (40)  Fanconi Syndrome [MESH:D005198] (253)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Bartter Syndrome [MESH:D001477] (241)   Bartter syndrome, antenatal type 1 [MESH:C537652] (39)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Hematuria [MESH:D006417] (477)  Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455) 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)  Urogenital Abnormalities [MESH:D014564] (2043)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Zellweger Syndrome [MESH:D015211] (182)  Diabetes Insipidus [MESH:D003919] (354)   Diabetes Insipidus, Neurogenic [MESH:D020790] (100)  Hyperoxaluria [MESH:D006959] (1498)   Hyperoxaluria, Primary [MESH:D006960] (63)   Primary hyperoxaluria type 1 [MESH:C536414] (48)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Donnai-Barrow syndrome [MESH:C536390] (40)  Fanconi Syndrome [MESH:D005198] (253)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Bartter Syndrome [MESH:D001477] (241)   Bartter syndrome, antenatal type 1 [MESH:C537652] (39)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Obstruction [MESH:D014517] (575)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Hematuria [MESH:D006417] (477)  Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) 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)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  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)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1M [MESH:C564390] (53)  Cardiomyopathies [MESH:D009202] (5331)   Systemic carnitine deficiency [MESH:C536778] (92)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1M [MESH:C564390] (53)  Heart Defects, Congenital [MESH:D006330] (2443)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Pulmonary Valve Stenosis [MESH:D011666] (360)   Keutel syndrome [MESH:C536167] (102)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Pulmonary Valve Stenosis [MESH:D011666] (109)   Keutel syndrome [MESH:C536167] (102)  Vascular Diseases [MESH:D014652] (8691)   Arteritis [MESH:D001167] (1084)  Hyperemia [MESH:D006940] (2372)  Peripheral Vascular Diseases [MESH:D016491] (1412)  Retinal Vein Occlusion [MESH:D012170] (607)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Dissecting [MESH:D000784] (699)   Loeys-Dietz Syndrome [MESH:D055947] (263)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Coronary Artery Disease [MESH:D003324] (2685)  Atherosclerosis [MESH:D050197] (4188)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  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)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2468)   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)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  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)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Thrombosis [MESH:D013927] (3101)   Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Venous Thrombosis [MESH:D020246] (1141)   Budd-Chiari Syndrome [MESH:D006502] (164)  Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)  Hypertension [MESH:D006973] (5655)   Hypertension, Malignant [MESH:D006974] (621)  Hypotension [MESH:D007022] (4045)   Shy-Drager Syndrome [MESH:D012791] (99)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Telangiectasis [MESH:D013684] (255)   Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084)  Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Methemoglobinemia [MESH:D008708] (850)  Anemia [MESH:D000740] (3966)   Anemia, Hemolytic [MESH:D000743] (3083)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Spherocytosis, Hereditary [MESH:D013103] (137)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  Blood Coagulation Disorders [MESH:D001778] (1828)   Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Factor V Deficiency [MESH:D005166] (61)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Coagulation Protein Disorders [MESH:D020147] (580)   Factor V Deficiency [MESH:D005166] (61)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Blood Protein Disorders [MESH:D001796] (3051)   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)   Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134)  Leukemia, Erythroblastic, Acute [MESH:D004915] (89)  Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  Hemorrhagic Disorders [MESH:D006474] (3359)   Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328)  Factor V Deficiency [MESH:D005166] (61)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)  Leukocyte Disorders [MESH:D007960] (2662)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Leukocytosis [MESH:D007964] (988)  Leukostasis [MESH:D018921] (769)  Eosinophilia [MESH:D004802] (537)   Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Polycythemia [MESH:D011086] (412)   Erythrocytosis, Familial, 3 [MESH:C565221] (48)  Thrombophilia [MESH:D019851] (592)   Thrombophilia, hereditary [MESH:C540694] (59)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Lymphatic Diseases [MESH:D008206] (5167)   Splenic Diseases [MESH:D013158] (1323)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  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, T-Cell [MESH:D016399] (1204)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Sarcoidosis [MESH:D012507] (895)   Sarcoidosis, Early-Onset [MESH:C563714] (16) 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)  Eye Abnormalities [MESH:D005124] (1233)  Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Keutel syndrome [MESH:C536167] (102)  Ulnar-mammary syndrome [MESH:C536937] (57)  Multiple pterygium syndrome [MESH:C537377] (23)  Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Netherton Syndrome [MESH:D056770] (43)  Zellweger Syndrome [MESH:D015211] (182)  Deaf-Blind Disorders [MESH:D054062] (132)   Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 [MESH:C566254] (93)  Vascular Malformations [MESH:D054079] (1108)   Telangiectasia, Hereditary Hemorrhagic [MESH:D013683] (75)  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)  Digestive System Abnormalities [MESH:D004065] (507)   Biliary Atresia [MESH:D001656] (68)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Arthrogryposis [MESH:D001176] (329)  Craniofacial Abnormalities [MESH:D019465] (3064)   Cleidocranial Dysplasia [MESH:D002973] (129)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Microcephaly [MESH:D008831] (700)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Plagiocephaly [MESH:D059041] (440)   Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Limb Deformities, Congenital [MESH:D017880] (1813)   Syndactyly [MESH:D013576] (487)  Hand Deformities, Congenital [MESH:D006228] (587)   Keutel syndrome [MESH:C536167] (102)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Syndactyly [MESH:D013576] (487)  Craniosynostoses [MESH:D003398] (438)   Craniosynostosis, Type 2 [MESH:C565753] (36)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Donnai-Barrow syndrome [MESH:C536390] (40)  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)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Skin Abnormalities [MESH:D012868] (1723)   Multiple pterygium syndrome [MESH:C537377] (23)  Ichthyosis [MESH:D007057] (481)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)  Netherton Syndrome [MESH:D056770] (43)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Oligodontia-Colorectal Cancer Syndrome [MESH:C563898] (48)  Urogenital Abnormalities [MESH:D014564] (2064)   Cryptorchidism [MESH:D003456] (215)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Pulmonary Alveolar Microlithiasis [MESH:C562405] (44)  Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Loeys-Dietz Syndrome [MESH:D055947] (263)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Spherocytosis, Hereditary [MESH:D013103] (137)  Thalassemia [MESH:D013789] (501)   beta-Thalassemia [MESH:D017086] (458)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324] (62)  Factor V Deficiency [MESH:D005166] (61)  Activated Protein C Resistance [MESH:D020016] (140)   Thrombophilia due to Activated Protein C Resistance [MESH:C566056] (59)  Dwarfism [MESH:D004392] (783)   Congenital Hypothyroidism [MESH:D003409] (266)   Thyroid Dyshormonogenesis 2A [MESH:C563206] (52)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Meretoja syndrome [MESH:C537459] (95)  Macular Dystrophy, Retinal, 2 [MESH:C562746] (63)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Cone-Rod Dystrophy 10 [MESH:C564597] (30)  Retinitis Pigmentosa 35 [MESH:C565206] (30)  Cone-Rod Dystrophy 12 [MESH:C567206] (63)  Retinitis Pigmentosa 41 [MESH:C567422] (63)  Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Allan-Herndon-Dudley syndrome [MESH:C537047] (24)  Mental Retardation, X-Linked 30 [MESH:C563146] (40)  Mental Retardation, X-Linked 91 [MESH:C564482] (7)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   beta-Thalassemia [MESH:D017086] (458)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Allan-Herndon-Dudley syndrome [MESH:C537047] (24)  Mental Retardation, X-Linked 30 [MESH:C563146] (40)  Mental Retardation, X-Linked 91 [MESH:C564482] (7)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Neurofibromatoses [MESH:D017253] (146)   Schwannomatosis [MESH:C536641] (29)  Neurofibromatosis 2 [MESH:D016518] (29)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Metabolism, Inborn Errors [MESH:D008661] (6032)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Malonic aciduria [MESH:C535702] (31)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Gamma aminobutyric acid transaminase deficiency [MESH:C535407] (61)  Beta ketothiolase deficiency [MESH:C535434] (65)  succinic semialdehyde dehydrogenase deficiency [MESH:C535803] (42)  Methylmalonic acidemia [MESH:C537358] (764)  Histidinemia [MESH:C538320] (87)  Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  2-Methylbutyryl-CoA Dehydrogenase Deficiency [MESH:C566487] (38)  Multiple Acyl Coenzyme A Dehydrogenase Deficiency [MESH:D054069] (88)  Phenylketonurias [MESH:D010661] (156)  Hyperhomocysteinemia [MESH:D020138] (1724)   Gamma-cystathionase deficiency [MESH:C535408] (106)  Homocystinuria [MESH:D006712] (93)  Multiple Carboxylase Deficiency [MESH:D009100] (51)   Biotinidase Deficiency [MESH:D028921] (31)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Galactosemias [MESH:D005693] (69)  Homocystinuria [MESH:D006712] (93)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Phenylketonurias [MESH:D010661] (156)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Peroxisomal Disorders [MESH:D018901] (1472)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Glucose-Galactose Malabsorption [MESH:C562602] (49)  Galactosemias [MESH:D005693] (69)  Fructose Metabolism, Inborn Errors [MESH:D015318] (125)   Fructose-1,6-Diphosphatase Deficiency [MESH:D015319] (72)  Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease 0, Liver [MESH:C565485] (45)  Glycogen Storage Disease 0, Muscle [MESH:C566917] (23)  Glycogen Storage Disease Type VI [MESH:D006013] (73)  Hyperoxaluria, Primary [MESH:D006960] (63)   Primary hyperoxaluria type 1 [MESH:C536414] (48)  Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Multiple Carboxylase Deficiency [MESH:D009100] (51)   Biotinidase Deficiency [MESH:D028921] (31)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  VLCAD deficiency [MESH:C536353] (55)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Sitosterolemia [MESH:C537345] (82)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)  Hypolipoproteinemias [MESH:D007009] (365)   Hypobetalipoproteinemias [MESH:D006995] (88)   Abetalipoproteinemia [MESH:D000012] (63)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, Type 2A [MESH:C566556] (72)  Hemochromatosis, Type 2B [MESH:C566557] (66)  Hypophosphatasia [MESH:D007014] (142)   Hypophosphatasia, Childhood [MESH:C562440] (137)  Hypophosphatasia, Infantile [MESH:C562646] (137)  Hypophosphatasia, Adult [MESH:C562647] (137)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Peroxisomal Disorders [MESH:D018901] (1788)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Acatalasia [MESH:D020642] (788)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Donnai-Barrow syndrome [MESH:C536390] (40)  Fanconi Syndrome [MESH:D005198] (253)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Duchenne [MESH:D020388] (942)  Myasthenic Syndromes, Congenital [MESH:D020294] (155)   Endplate Acetylcholinesterase Deficiency [MESH:C566415] (16)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Hemangioma, capillary infantile [MESH:C535860] (190)  Meningioma, familial [MESH:C537443] (195)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Wilms Tumor [MESH:D009396] (553)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Neurofibromatoses [MESH:D017253] (146)   Schwannomatosis [MESH:C536641] (29)  Neurofibromatosis 2 [MESH:D016518] (29)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)  Erythrokeratodermia Variabilis [MESH:D056266] (26)  Netherton Syndrome [MESH:D056770] (43)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)  Netherton Syndrome [MESH:D056770] (43)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal [MESH:C563463] (52)  Diabetes Mellitus, Transient Neonatal, 2 [MESH:C563672] (42)  Asphyxia Neonatorum [MESH:D001238] (1648)  Congenital Hyperinsulinism [MESH:D044903] (132)  Ichthyosis [MESH:D007057] (476)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)  Netherton Syndrome [MESH:D056770] (43)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Infant, Premature, Diseases [MESH:D007235] (1292)   Bronchopulmonary Dysplasia [MESH:D001997] (1021) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  Homocystinuria [MESH:D006712] (93)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Cartilage Diseases [MESH:D002357] (438)   Keutel syndrome [MESH:C536167] (102)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  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)  Drug Eruptions [MESH:D003875] (2697)  Eczema [MESH:D004485] (235)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Erythema [MESH:D004890] (1330)   Erythrokeratodermia Variabilis [MESH:D056266] (26)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Woolly hair, congenital [MESH:C536745] (20)  Hypotrichosis [MESH:D007039] (1513)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Alopecia [MESH:D000505] (1453)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Keratosis [MESH:D007642] (1941)   Erythrokeratodermia Variabilis [MESH:D056266] (26)  Ichthyosis [MESH:D007057] (481)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)  Netherton Syndrome [MESH:D056770] (43)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Pigmentation Disorders [MESH:D010859] (1215)   Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Skin Abnormalities [MESH:D012868] (1709)   Multiple pterygium syndrome [MESH:C537377] (23)  Ichthyosis [MESH:D007057] (481)   Ichthyosis with hypotrichosis, autosomal recessive [MESH:C536273] (32)  Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)  Netherton Syndrome [MESH:D056770] (43)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  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)  Erythrokeratodermia Variabilis [MESH:D056266] (26)  Netherton Syndrome [MESH:D056770] (43)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Hyperkeratosis, Epidermolytic [MESH:D017488] (136)  Netherton Syndrome [MESH:D056770] (43)  Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Skin Neoplasms [MESH:D012878] (2991)   Schwannomatosis [MESH:C536641] (29) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Z. Exceptions (817)   Not Fully Specified [NFS] (817)  Metabolic Diseases [MESH:D008659] (9025)   Acid-Base Imbalance [MESH:D000137] (854)   Acidosis [MESH:D000138] (626)   Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Galactosemias [MESH:D005693] (69)  Homocystinuria [MESH:D006712] (93)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Phenylketonurias [MESH:D010661] (156)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Peroxisomal Disorders [MESH:D018901] (1472)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Calcinosis [MESH:D002114] (2989)   Keutel syndrome [MESH:C536167] (102)  Pulmonary Alveolar Microlithiasis [MESH:C562405] (44)  Vascular Calcification [MESH:D061205] (138)  Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321)  Diabetes Mellitus, Transient Neonatal, 2 [MESH:C563672] (42)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Congenital Hyperinsulinism [MESH:D044903] (132)  Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Hypoglycemia [MESH:D007003] (2420)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Hypoglycemia, leucine-induced [MESH:C537150] (43)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Congenital Hyperinsulinism [MESH:D044903] (132)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, Type 2A [MESH:C566556] (72)  Hemochromatosis, Type 2B [MESH:C566557] (66)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)   Sitosterolemia [MESH:C537345] (82)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Hypertriglyceridemia [MESH:D015228] (808)   Hyperlipoproteinemia Type V [MESH:D006954] (37)  Hypolipoproteinemias [MESH:D007009] (409)   Hypobetalipoproteinemias [MESH:D006995] (181)   Abetalipoproteinemia [MESH:D000012] (63)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  VLCAD deficiency [MESH:C536353] (55)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Sitosterolemia [MESH:C537345] (82)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Xanthomatosis [MESH:D014973] (145)   Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)  Malabsorption Syndromes [MESH:D008286] (1869)   Glucose-Galactose Malabsorption [MESH:C562602] (49)  Celiac Disease [MESH:D002446] (340)  Hyperhomocysteinemia [MESH:D020138] (1716)   Gamma-cystathionase deficiency [MESH:C535408] (106)  Steatorrhea [MESH:D045602] (41)   Bile Acid Malabsorption, Primary [MESH:C567652] (38)  Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Metabolism, Inborn Errors [MESH:D008661] (6028)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Malonic aciduria [MESH:C535702] (31)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Gamma aminobutyric acid transaminase deficiency [MESH:C535407] (61)  Beta ketothiolase deficiency [MESH:C535434] (65)  succinic semialdehyde dehydrogenase deficiency [MESH:C535803] (42)  Methylmalonic acidemia [MESH:C537358] (764)  Histidinemia [MESH:C538320] (87)  Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  2-Methylbutyryl-CoA Dehydrogenase Deficiency [MESH:C566487] (38)  Multiple Acyl Coenzyme A Dehydrogenase Deficiency [MESH:D054069] (88)  Phenylketonurias [MESH:D010661] (156)  Hyperhomocysteinemia [MESH:D020138] (1724)   Gamma-cystathionase deficiency [MESH:C535408] (106)  Homocystinuria [MESH:D006712] (93)  Multiple Carboxylase Deficiency [MESH:D009100] (51)   Biotinidase Deficiency [MESH:D028921] (31)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Galactosemias [MESH:D005693] (69)  Homocystinuria [MESH:D006712] (93)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Phenylketonurias [MESH:D010661] (156)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Peroxisomal Disorders [MESH:D018901] (1472)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Glucose-Galactose Malabsorption [MESH:C562602] (49)  Galactosemias [MESH:D005693] (69)  Fructose Metabolism, Inborn Errors [MESH:D015318] (125)   Fructose-1,6-Diphosphatase Deficiency [MESH:D015319] (72)  Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease 0, Liver [MESH:C565485] (45)  Glycogen Storage Disease 0, Muscle [MESH:C566917] (23)  Glycogen Storage Disease Type VI [MESH:D006013] (73)  Hyperoxaluria, Primary [MESH:D006960] (63)   Primary hyperoxaluria type 1 [MESH:C536414] (48)  Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Multiple Carboxylase Deficiency [MESH:D009100] (51)   Biotinidase Deficiency [MESH:D028921] (31)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  VLCAD deficiency [MESH:C536353] (55)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Sitosterolemia [MESH:C537345] (82)  Carnitine-Acylcarnitine Translocase Deficiency [MESH:C562812] (51)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Hyperlipoproteinemia Type V [MESH:D006954] (37)  Xanthomatosis, Cerebrotendinous [MESH:D019294] (90)  Hypolipoproteinemias [MESH:D007009] (365)   Hypobetalipoproteinemias [MESH:D006995] (88)   Abetalipoproteinemia [MESH:D000012] (63)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Mucolipidoses [MESH:D009081] (78)   Mucolipidosis III Gamma [MESH:C565367] (13)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Molybdenum cofactor deficiency [MESH:C535811] (57)  Hemochromatosis [MESH:D006432] (1694)   Hemochromatosis, Type 2A [MESH:C566556] (72)  Hemochromatosis, Type 2B [MESH:C566557] (66)  Hypophosphatasia [MESH:D007014] (142)   Hypophosphatasia, Childhood [MESH:C562440] (137)  Hypophosphatasia, Infantile [MESH:C562646] (137)  Hypophosphatasia, Adult [MESH:C562647] (137)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Peroxisomal Disorders [MESH:D018901] (1788)   Peroxisome biogenesis disorders [MESH:C536664] (101)  Acatalasia [MESH:D020642] (788)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Donnai-Barrow syndrome [MESH:C536390] (40)  Fanconi Syndrome [MESH:D005198] (253)  Acidosis, Renal Tubular [MESH:D000141] (225)   Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Mitochondrial Diseases [MESH:D028361] (2561)   VLCAD deficiency [MESH:C536353] (55)  Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal [MESH:C563463] (52)  3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Multiple Acyl Coenzyme A Dehydrogenase Deficiency [MESH:D054069] (88)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)   Hypophosphatemia, Familial [MESH:D007015] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Meretoja syndrome [MESH:C537459] (95)  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, Sporadic [MESH:C566291] (239)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Dehydration [MESH:D003681] (121)  Hypercalcemia [MESH:D006934] (1999)  Hyperkalemia [MESH:D006947] (485)  Hyponatremia [MESH:D007010] (789)  Inappropriate ADH Syndrome [MESH:D007177] (178)  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)   Gamma-cystathionase deficiency [MESH:C535408] (106)  Vitamin D Deficiency [MESH:D014808] (360)   Rickets [MESH:D012279] (341)   Rickets, Hypophosphatemic [MESH:D063730] (276)   Familial Hypophosphatemic Rickets [MESH:D053098] (274)   Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Hyperaldosteronism [MESH:D006929] (419)   Bartter Syndrome [MESH:D001477] (241)   Bartter syndrome, antenatal type 1 [MESH:C537652] (39)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321)  Diabetes Mellitus, Transient Neonatal, 2 [MESH:C563672] (42)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Dwarfism [MESH:D004392] (698)   Congenital Hypothyroidism [MESH:D003409] (266)   Thyroid Dyshormonogenesis 2A [MESH:C563206] (52)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Multiple Endocrine Neoplasia [MESH:D009377] (375)   Multiple Endocrine Neoplasia Type 2a [MESH:D018813] (102)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Neoplasms [MESH:D013964] (2040)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Gonadal Disorders [MESH:D006058] (5088)   Hypogonadism [MESH:D007006] (1123)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  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 Microlithiasis [MESH:C566478] (44)  Cryptorchidism [MESH:D003456] (215)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Pituitary Diseases [MESH:D010900] (1829)   Hypopituitarism [MESH:D007018] (732)  Inappropriate ADH Syndrome [MESH:D007177] (178)  Diabetes Insipidus [MESH:D003919] (302)   Diabetes Insipidus, Neurogenic [MESH:D020790] (100)  Hyperpituitarism [MESH:D006964] (1259)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Gigantism [MESH:D005877] (46)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Pituitary Neoplasms [MESH:D010911] (981)   Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)  Hypothyroidism [MESH:D007037] (496)   Congenital Hypothyroidism [MESH:D003409] (266)   Thyroid Dyshormonogenesis 2A [MESH:C563206] (52)  Thyroid Neoplasms [MESH:D013964] (2040)   Familial medullary thyroid carcinoma [MESH:C536911] (101)  Thyroiditis [MESH:D013966] (158)   Thyroiditis, Autoimmune [MESH:D013967] (149)   Hashimoto Disease [MESH:D050031] (98) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  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)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Anaphylaxis [MESH:D000707] (299)  Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Lymphopenia [MESH:D008231] (990)  HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  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 B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  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, T-Cell [MESH:D016399] (1382)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Mammary Neoplasms, Animal [MESH:D015674] (2735)  Paratuberculosis [MESH:D010283] (427) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Ventricular Remodeling [MESH:D020257] (686)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Donnai-Barrow syndrome [MESH:C536390] (40)  Alopecia [MESH:D000505] (1383)   Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis [MESH:C564365] (78)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)   Allan-Herndon-Dudley syndrome [MESH:C537047] (24)  Calculi [MESH:D002137] (756)   Testicular Microlithiasis [MESH:C566478] (44)  Gallstones [MESH:D042882] (350)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Encephalocele [MESH:D004677] (151)   Parietal Foramina With Cleidocranial Dysplasia [MESH:C566825] (36)  Parietal Foramina [MESH:C566826] (42)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Chromosome Aberrations [MESH:D002869] (2352)  Dehydration [MESH:D003681] (121)  Gliosis [MESH:D005911] (1419)  Growth Disorders [MESH:D006130] (2438)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Leukocytosis [MESH:D007964] (978)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Hemorrhage [MESH:D006470] (4451)   Gastrointestinal Hemorrhage [MESH:D006471] (815)  Hematuria [MESH:D006417] (477)  Shock, Hemorrhagic [MESH:D012771] (2042)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Hyperammonemia [MESH:D022124] (322)   Systemic carnitine deficiency [MESH:C536778] (92)  Inflammation [MESH:D007249] (5241)   Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Intraoperative Complications [MESH:D007431] (131)   Malignant Hyperthermia [MESH:D008305] (92)   Multiple pterygium syndrome [MESH:C537377] (23)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Dysmenorrhea [MESH:D004412] (189)  Oligomenorrhea [MESH:D009839] (228)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   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)   Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Reflex, Abnormal [MESH:D012021] (485)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (984)   Cerebellar Ataxia [MESH:D002524] (289)   Dysequilibrium syndrome [MESH:C535731] (83)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Dysequilibrium syndrome [MESH:C535731] (83)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Histidinemia [MESH:C538320] (87)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Muscle Hypotonia [MESH:D009123] (258)   Allan-Herndon-Dudley syndrome [MESH:C537047] (24)  Muscular Atrophy [MESH:D009133] (1234)   Allan-Herndon-Dudley syndrome [MESH:C537047] (24)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Seizures [MESH:D012640] (4502)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Donnai-Barrow syndrome [MESH:C536390] (40)  Deafness, Autosomal Recessive 1A [MESH:C567134] (88)  Deafness, Autosomal Dominant 2B [MESH:C567214] (18)  Deafness, Autosomal Dominant 2A [MESH:C567441] (36)  Usher Syndromes [MESH:D052245] (83)   Usher syndrome, type 1C [MESH:C536486] (15)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Pelvic Pain [MESH:D017699] (198)   Dysmenorrhea [MESH:D004412] (189)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Hyperphagia [MESH:D006963] (206)  Vomiting [MESH:D014839] (1354)  Diarrhea [MESH:D003967] (858)   Bile Acid Malabsorption, Primary [MESH:C567652] (38)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Respiratory Sounds [MESH:D012135] (713)  Urological Manifestations [MESH:D020924] (3532)   Polyuria [MESH:D011141] (279)  Hypercalciuria [MESH:D053565] (330)   Hypercalciuria, Absorptive, 2 [MESH:C562790] (15)  Hypophosphatemic Rickets with Hypercalciuria, Hereditary [MESH:C562793] (17)  Proteinuria [MESH:D011507] (3293)   Donnai-Barrow syndrome [MESH:C536390] (40)  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)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Cadmium Poisoning [MESH:D002105] (180)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Manganese Poisoning [MESH:D020149] (2214)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Drug Overdose [MESH:D062787] (513)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Neoplasms, Radiation-Induced [MESH:D009381] (171)  Radiation Injuries, Experimental [MESH:D011833] (2662)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Carboxylic Acids [MESH:D002264] (13103)   Acids, Carbocyclic [MESH:D000146] (5074)   Phenylpropionates [MESH:D010666] (285)  Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Acyclic [MESH:D006839] (3563)   Alkanes [MESH:D000473] (1061)   Alkanesulfonic Acids [MESH:D017738] (356)   Alkanesulfonates [MESH:D000476] (203)  Sulfur Compounds [MESH:D013457] (10450)   Sulfur Acids [MESH:D013456] (1159)   Sulfonic Acids [MESH:D013451] (990)   Alkanesulfonic Acids [MESH:D017738] (374)   Alkanesulfonates [MESH:D000476] (221) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Diagnostic Imaging [MESH:D003952] (623)   Ultrasonography [MESH:D014463] (482)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Diagnostic Techniques, Cardiovascular [MESH:D003935] (521)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457) 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)   Dysequilibrium syndrome [MESH:C535731] (83)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Histidinemia [MESH:C538320] (87)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Psychomotor Disorders [MESH:D011596] (250)   Phosphoserine Aminotransferase Deficiency [MESH:C567032] (85)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Dysequilibrium syndrome [MESH:C535731] (83)  Simpson-Golabi-Behmel syndrome [MESH:C537340] (45)  Histidinemia [MESH:C538320] (87)  Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation [MESH:C567038] (48)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XY Disorders of Sex Development [MESH:D058490] (388)   Persistent Mullerian duct syndrome [MESH:C536665] (47)  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) G. Phenomena and Processes  G. Phenomena and Processes  Circulatory and Respiratory Physiological Phenomena [MESH:D002943] (614)   Cardiovascular Physiological Phenomena [MESH:D002320] (525)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)