Item 5 of 7 (back to results) previous next   Tetracycline D013752               MeSH Unique Identifier: D013752 Scope Notes: A naphthacene antibiotic that inhibits AMINO ACYL TRNA binding during protein synthesis. Chemical – Gene Interaction Note 1: ABCC4 protein results in increased transport of Tetracycline Note 2: Tetracycline results in decreased expression of AP1S1 mRNA Click here for more information

Current search: C23. Pathological Conditions, Signs and Symptoms: Pathological Conditions, Anatomical [MESH:D020763] > Cysts [MESH:D003560] > Spermatocele [MESH:D013088] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily C [HGNC:ABCC] (458)   ATP-binding cassette, sub-family C (CFTR/MRP), member 4 [HGNC:ABCC4] (88)  CD molecules [HGNC:CD] (1459)   prion protein [HGNC:PRNP] (49)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612)  Fibronectin type III domain containing [HGNC:FN3] (399)   fibronectin type III domain containing 4 [HGNC:FNDC4] (25)  Glutathione S-transferases [HGNC:GST] (460)   Glutathione S-transferases, soluble [HGNC:SGST] (447)   glutathione S-transferase mu 3 (brain) [HGNC:GSTM3] (41)  glutathione S-transferase pi 1 [HGNC:GSTP1] (218)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 01, beta [HGNC:IL1B] (497)  Solute carriers [HGNC:SLC] (716)   solute carrier family 22 (organic anion transporter), member 06 [HGNC:SLC22A6] (72)  solute carrier family 22 (organic anion transporter), member 08 [HGNC:SLC22A8] (42)  WD repeat domain containing [HGNC:WDR] (199)   WD repeat domain, phosphoinositide interacting 1 [HGNC:WIPI1] (42) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  metabolic processing (485)  Decreases (5154)   activity (2549)  expression (2187)  reaction (3393)  Increases (5571)   activity (2865)  export (105)  expression (3238)  transport (399)  uptake (378) A. Anatomy  A. Anatomy  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Spine [MESH:D013131] (258)   VACTERL hydrocephaly [MESH:C536521] (151)  Digestive System [MESH:D004064] (421)   Gastrointestinal Tract [MESH:D041981] (364)   Intestines [MESH:D007422] (271)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Lower Gastrointestinal Tract [MESH:D041741] (254)   Intestine, Large [MESH:D007420] (247)   Anal Canal [MESH:D001003] (217)   VACTERL hydrocephaly [MESH:C536521] (151)  Upper Gastrointestinal Tract [MESH:D041742] (236)   Esophagus [MESH:D004947] (200)   VACTERL hydrocephaly [MESH:C536521] (151)  Respiratory System [MESH:D012137] (321)   Trachea [MESH:D014132] (190)   VACTERL hydrocephaly [MESH:C536521] (151)  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   VACTERL hydrocephaly [MESH:C536521] (151)  Sense Organs [MESH:D012679] (1060)   Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Cornea [MESH:D003315] (40)   Cornea Plana 2 [MESH:C565677] (9)  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 16-18 [MESH:D002902] (799)   Chromosomes, Human, Pair 17 [MESH:D002886] (779)   Chromosome 17 deletion [MESH:C538045] (769) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Brucellosis [MESH:D002006] (4)  Helicobacter Infections [MESH:D016481] (579)  Enterobacteriaceae Infections [MESH:D004756] (669)   Escherichia coli Infections [MESH:D004927] (40)  Proteus Infections [MESH:D011512] (18)  Pasteurellaceae Infections [MESH:D016871] (348)   Haemophilus Infections [MESH:D006192] (44)  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)  Streptococcal Infections [MESH:D013290] (158)   Pneumococcal Infections [MESH:D011008] (122)  Infection [MESH:D007239] (4109)   Respiratory Tract Infections [MESH:D012141] (199)  Urinary Tract Infections [MESH:D014552] (984)  Sepsis [MESH:D018805] (3556)   Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Poliomyelitis [MESH:D011051] (54)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Myelitis [MESH:D009187] (71)   Poliomyelitis [MESH:D011051] (56)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Picornaviridae Infections [MESH:D010850] (1672)   Enterovirus Infections [MESH:D004769] (241)   Poliomyelitis [MESH:D011051] (56)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   HIV Seropositivity [MESH:D006679] (480)  HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   HIV Seropositivity [MESH:D006679] (480)  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)   Liver Diseases, Parasitic [MESH:D008109] (1009)  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)   Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  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)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Lipoma [MESH:D008067] (159)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Myoma [MESH:D009214] (203)   Rhabdomyoma [MESH:D012207] (200)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  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)   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)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Lewis Lung [MESH:D018827] (248)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   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)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   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)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangioma [MESH:D006391] (690)  Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Nevus [MESH:D009506] (340)   Nevus, Pigmented [MESH:D009508] (123)   Nevus, Epidermal [MESH:C562736] (112)  Neoplasms by Site [MESH:D009371] (9169)   Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Digestive System Neoplasms [MESH:D004067] (7487)   Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Thyroid Neoplasms [MESH:D013964] (2040)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Thyroid Neoplasms [MESH:D013964] (2040)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Nose Neoplasms [MESH:D009669] (390)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Skin Neoplasms [MESH:D012878] (2992)   Nevus, Epidermal [MESH:C562736] (112)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Carcinoma, Lewis Lung [MESH:D018827] (248)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Hamartoma Syndrome, Multiple [MESH:D006223] (262)   Proteus Syndrome [MESH:D016715] (152)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Paraneoplastic Syndromes [MESH:D010257] (231)   Paraneoplastic Endocrine Syndromes [MESH:D009384] (207)   ACTH Syndrome, Ectopic [MESH:D000182] (200)  Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)   Osteitis Deformans [MESH:D010001] (287)  Bone Diseases, Developmental [MESH:D001848] (3315)   Marfan Syndrome [MESH:D008382] (646)  Proteus Syndrome [MESH:D016715] (152)  Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Osteochondrodysplasias [MESH:D010009] (2440)   Spondyloepimetaphyseal Dysplasia, Missouri Type [MESH:C566574] (142)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Neoplasms [MESH:D001859] (1334)   Skull Neoplasms [MESH:D012888] (399)   Nose Neoplasms [MESH:D009669] (384)  Osteonecrosis [MESH:D010020] (539)   Femur Head Necrosis [MESH:D005271] (268)  Jaw Diseases [MESH:D007571] (1601)   Mandibular Diseases [MESH:D008336] (395)  Maxillary Diseases [MESH:D008439] (354)  Joint Diseases [MESH:D007592] (4657)   Synovitis [MESH:D013585] (270)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Chondrocalcinosis [MESH:D002805] (213)  Osteoarthritis [MESH:D010003] (1743)  Sacroiliitis [MESH:D058566] (202)  Gout [MESH:D006073] (261)   Arthritis, Gouty [MESH:D015210] (211)  Muscular Diseases [MESH:D009135] (4071)   Muscle Weakness [MESH:D018908] (478)  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] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   LEOPARD Syndrome [MESH:D044542] (299)  Microcephaly [MESH:D008831] (700)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Limb Deformities, Congenital [MESH:D017880] (1813)   VACTERL hydrocephaly [MESH:C536521] (151)  Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Polydactyly [MESH:D017689] (318)  Proteus Syndrome [MESH:D016715] (152)  Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Gout [MESH:D006073] (261)   Arthritis, Gouty [MESH:D015210] (211) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Bile acid synthesis defect, congenital, 1 [MESH:C535442] (25)  Bile acid synthesis defect, congenital, 2 [MESH:C535443] (51)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Cholestasis, progressive familial intrahepatic 2 [MESH:C535934] (190)  Alagille Syndrome [MESH:D016738] (105)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Cholelithiasis [MESH:D002769] (373)   Gallstones [MESH:D042882] (350)  Gallbladder Diseases [MESH:D005705] (1215)   Cholecystolithiasis [MESH:D041761] (353)   Gallstones [MESH:D042882] (350)  Digestive System Neoplasms [MESH:D004067] (7493)   Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  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)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Duodenal Diseases [MESH:D004378] (1982)   Peptic Ulcer [MESH:D010437] (1969)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   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)   Glycogen Storage Disease 0, Liver [MESH:C565485] (45)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Zellweger Syndrome [MESH:D015211] (182)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Cholestasis, progressive familial intrahepatic 1 [MESH:C535933] (263)  Cholestasis, progressive familial intrahepatic 2 [MESH:C535934] (190)  Alagille Syndrome [MESH:D016738] (105)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis B, Chronic [MESH:D019694] (277)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Hepatitis B [MESH:D006509] (976)   Hepatitis B, Chronic [MESH:D019694] (277)  Liver Cirrhosis [MESH:D008103] (5542)   Cirrhosis, Familial [MESH:C566123] (179)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Mandibular Diseases [MESH:D008336] (450)  Maxillary Diseases [MESH:D008439] (354)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mucositis [MESH:D052016] (1238)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Facial Paralysis [MESH:D005158] (238)   Aortic Arch Interruption, Facial Palsy, and Retinal Coloboma [MESH:C566271] (157)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Periodontal Diseases [MESH:D010510] (1001)   Periodontitis [MESH:D010518] (843)   Periodontitis, Aggressive, 2 [MESH:C566946] (310)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Tooth Abnormalities [MESH:D014071] (622)   Tooth Agenesis, Selective, 6 [MESH:C567755] (154)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Tooth Agenesis, Selective, 6 [MESH:C567755] (154) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Bronchitis [MESH:D001991] (993)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Idiopathic Interstitial Pneumonias [MESH:D054988] (314)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pulmonary Fibrosis [MESH:D011658] (3140)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Pleural Diseases [MESH:D010995] (2240)   Pleural Effusion [MESH:D010996] (39)  Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Respiratory Tract Infections [MESH:D012141] (3926)   Bronchitis [MESH:D001991] (588)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Nose Neoplasms [MESH:D009669] (390)  Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Nose Diseases [MESH:D009668] (1504)   Nose Neoplasms [MESH:D009669] (390)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Nose Neoplasms [MESH:D009669] (390)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Restless Legs Syndrome [MESH:D012148] (379)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  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)  Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)   Hypotension, Orthostatic [MESH:D007024] (679)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Brain Damage, Chronic [MESH:D001925] (311)   Cerebral Palsy [MESH:D002547] (300)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Peroxisomal Disorders [MESH:D018901] (1472)   Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial 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)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Spasms, Infantile [MESH:D013036] (468)  Hydrocephalus [MESH:D006849] (276)   VACTERL hydrocephaly [MESH:C536521] (151)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Hypopituitarism [MESH:D007018] (732)  Hyperpituitarism [MESH:D006964] (1250)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Intracranial Hypertension [MESH:D019586] (368)   Hydrocephalus [MESH:D006849] (274)   VACTERL hydrocephaly [MESH:C536521] (151)  Pseudotumor Cerebri [MESH:D011559] (46)   Idiopathic intracranial hypertension with papilledema [MESH:C531795] (8)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  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)   Poliomyelitis [MESH:D011051] (56)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Myelitis [MESH:D009187] (69)   Poliomyelitis [MESH:D011051] (54)  Meningitis [MESH:D008581] (1506)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Myelitis [MESH:D009187] (69)   Poliomyelitis [MESH:D011051] (54)  Prion Diseases [MESH:D017096] (488)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Ocular Motility Disorders [MESH:D015835] (364)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Spinal Cord Diseases [MESH:D013118] (4376)   Poliomyelitis [MESH:D011051] (55)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Myelitis [MESH:D009187] (75)   Poliomyelitis [MESH:D011051] (54)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)   Papilledema [MESH:D010211] (50)  Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  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)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neurocutaneous Syndromes [MESH:D020752] (1230)   von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  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 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Prion Diseases [MESH:D017096] (475)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Ataxia [MESH:D001259] (1138)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Myoclonus [MESH:D009207] (427)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Facial Paralysis [MESH:D005158] (238)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5011)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (501)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Diplopia [MESH:D004172] (59)  Neuromuscular Diseases [MESH:D009468] (7336)   Poliomyelitis [MESH:D011051] (55)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Muscular Diseases [MESH:D009135] (3538)   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)   Myasthenia Gravis [MESH:D009157] (632)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Neuritis [MESH:D009443] (55)  Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Mononeuropathies [MESH:D020422] (604)   Median Neuropathy [MESH:D020423] (153)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Nerve Compression Syndromes [MESH:D009408] (166)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Polyneuropathies [MESH:D011115] (1134)   Tangier Disease [MESH:D013631] (170)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  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)   Restless Legs Syndrome [MESH:D012148] (379)  Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)   Insomnia, Fatal Familial [MESH:D034062] (98)  Parasomnias [MESH:D020447] (453)   Restless Legs Syndrome [MESH:D012148] (379)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Z. Exceptions (245)   Not Fully Specified [NFS] (245)  Eye Diseases [MESH:D005128] (6245)   Eye Abnormalities [MESH:D005124] (1233)  Conjunctival Diseases [MESH:D003229] (273)   Conjunctivitis [MESH:D003231] (133)   Plasminogen Deficiency, Type I [MESH:C566897] (83)  Corneal Diseases [MESH:D003316] (1445)   Cornea Plana 2 [MESH:C565677] (9)  Corneal Opacity [MESH:D003318] (544)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Cornea Plana 2 [MESH:C565677] (9)  Graves Ophthalmopathy [MESH:D049970] (165)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (414)   Retinitis Pigmentosa 37 [MESH:C567005] (11)  Eye Manifestations [MESH:D005132] (208)   Eye Pain [MESH:D058447] (207)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)  Ocular Motility Disorders [MESH:D015835] (1699)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)   Papilledema [MESH:D010211] (50)  Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Refractive Errors [MESH:D012030] (457)   Anisometropia [MESH:D015858] (152)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Degeneration [MESH:D012162] (2386)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Retinitis Pigmentosa 37 [MESH:C567005] (11)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784)  Vision Disorders [MESH:D014786] (534)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Diplopia [MESH:D004172] (59) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Spermatocele [MESH:D013088] (7)  Testicular Hydrocele [MESH:D006848] (3)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)  Penile Diseases [MESH:D010409] (1805)   Penile Neoplasms [MESH:D010412] (890)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Urogenital Abnormalities [MESH:D014564] (2065)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetes Insipidus [MESH:D003919] (354)  Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Kidney Diseases, Cystic [MESH:D052177] (1009)  Nephrocalcinosis [MESH:D009397] (311)  Zellweger Syndrome [MESH:D015211] (182)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Pyelonephritis [MESH:D011704] (35)  Pyelitis [MESH:D011702] (37)   Pyelonephritis [MESH:D011704] (35)  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)   Fanconi Syndrome [MESH:D005198] (253)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  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)   Anuria [MESH:D001002] (833)  Hematuria [MESH:D006417] (477)  Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)  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)   Endometrial Hyperplasia [MESH:D004714] (263)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Abnormalities [MESH:D014564] (2043)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetes Insipidus [MESH:D003919] (354)  Diabetic Nephropathies [MESH:D003928] (2301)  Fanconi Syndrome [MESH:D005198] (253)  Hepatorenal Syndrome [MESH:D006530] (910)  Kidney Diseases, Cystic [MESH:D052177] (1009)  Nephrocalcinosis [MESH:D009397] (311)  Zellweger Syndrome [MESH:D015211] (182)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Lupus Nephritis [MESH:D008181] (602)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Pyelonephritis [MESH:D011704] (35)  Pyelitis [MESH:D011702] (37)   Pyelonephritis [MESH:D011704] (35)  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)   Fanconi Syndrome [MESH:D005198] (253)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  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)   Anuria [MESH:D001002] (833)  Hematuria [MESH:D006417] (477)  Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)  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)   Diabetes, Gestational [MESH:D016640] (1157)  Abortion, Spontaneous [MESH:D000022] (2780)   Embryo Loss [MESH:D020964] (288)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  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)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   VACTERL hydrocephaly [MESH:C536521] (151)  Alagille Syndrome [MESH:D016738] (105)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Tetralogy of Fallot [MESH:D013771] (121)  Transposition of Great Vessels [MESH:D014188] (60)  Heart Diseases [MESH:D006331] (8614)   Glycogen Storage Disease of Heart, Lethal Congenital [MESH:C564888] (30)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Bradycardia [MESH:D001919] (1899)  Long QT Syndrome [MESH:D008133] (693)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Heart Block [MESH:D006327] (571)   Sick Sinus Syndrome [MESH:D012804] (293)  Pre-Excitation Syndromes [MESH:D011226] (43)   Wolff-Parkinson-White Syndrome [MESH:D014927] (40)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 6 [MESH:C563436] (30)  Heart Defects, Congenital [MESH:D006330] (2443)   VACTERL hydrocephaly [MESH:C536521] (151)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Tetralogy of Fallot [MESH:D013771] (121)  Transposition of Great Vessels [MESH:D014188] (60)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   LEOPARD Syndrome [MESH:D044542] (299)  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 Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Stenosis, Subvalvular [MESH:D001020] (203)  Vascular Diseases [MESH:D014652] (8691)   Angioedema [MESH:D000799] (837)  Arteritis [MESH:D001167] (1084)  Hyperemia [MESH:D006940] (2372)  Peripheral Vascular Diseases [MESH:D016491] (1412)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Aneurysm, Ruptured [MESH:D017542] (645)   Aortic Rupture [MESH:D001019] (637)  Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Aortic Diseases [MESH:D001018] (1737)   Aortic Aneurysm [MESH:D001014] (1721)   Aortic Aneurysm, Thoracic [MESH:D017545] (781)  Aortic Rupture [MESH:D001019] (637)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial 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)  Thrombosis [MESH:D013927] (3101)   Venous Thrombosis [MESH:D020246] (1141)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypertension [MESH:D006973] (5655)   Hypertension, Malignant [MESH:D006974] (621)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  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)   Adenosine Triphosphate, Elevated, Of Erythrocytes [MESH:C566310] (78)  Anemia [MESH:D000740] (3966)   Anemia, Aplastic [MESH:D000741] (1925)  Anemia, Hemolytic [MESH:D000743] (3083)   Anemia, Hemolytic, Autoimmune [MESH:D000744] (117)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, hypochromic microcytic [MESH:C536357] (164)  Anemia, Macrocytic [MESH:D000748] (382)   Anemia, Megaloblastic [MESH:D000749] (288)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Coagulation Protein Disorders [MESH:D020147] (580)   Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Blood Protein Disorders [MESH:D001796] (3051)   Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)  Myelodysplastic Syndromes [MESH:D009190] (2093)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Leukocyte Disorders [MESH:D007960] (2662)   Leukocytosis [MESH:D007964] (988)  Leukostasis [MESH:D018921] (769)  Leukopenia [MESH:D007970] (1921)   Lymphopenia [MESH:D008231] (990)  Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Methemoglobinemia [MESH:D008708] (850)   NADH cytochrome B5 reductase deficiency [MESH:C537841] (66)  Thrombophilia [MESH:D019851] (592)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphedema [MESH:D008209] (162)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  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)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Drug-Induced [MESH:D000014] (1024)  Eye Abnormalities [MESH:D005124] (1233)  Abnormalities, Multiple [MESH:D000015] (3192)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Alagille Syndrome [MESH:D016738] (105)  LEOPARD Syndrome [MESH:D044542] (299)  Marfan Syndrome [MESH:D008382] (646)  Proteus Syndrome [MESH:D016715] (152)  Zellweger Syndrome [MESH:D015211] (182)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   VACTERL hydrocephaly [MESH:C536521] (151)  Alagille Syndrome [MESH:D016738] (105)  LEOPARD Syndrome [MESH:D044542] (299)  Long QT Syndrome [MESH:D008133] (693)  Marfan Syndrome [MESH:D008382] (646)  Tetralogy of Fallot [MESH:D013771] (121)  Transposition of Great Vessels [MESH:D014188] (60)  Wolff-Parkinson-White Syndrome [MESH:D014927] (40)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   LEOPARD Syndrome [MESH:D044542] (299)  Microcephaly [MESH:D008831] (700)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Limb Deformities, Congenital [MESH:D017880] (1813)   VACTERL hydrocephaly [MESH:C536521] (151)  Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Polydactyly [MESH:D017689] (318)  Proteus Syndrome [MESH:D016715] (152)  Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Synostosis [MESH:D013580] (817)   Syndactyly [MESH:D013576] (487)   Syndactyly Cenani Lenz type [MESH:C538150] (26)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Macrocephaly [MESH:D058627] (264)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)  Skin Abnormalities [MESH:D012868] (1723)   Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Tooth Abnormalities [MESH:D014071] (622)  Urogenital Abnormalities [MESH:D014564] (2064)   Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Cirrhosis, Familial [MESH:C566123] (179)  Alagille Syndrome [MESH:D016738] (105)  Cystic Fibrosis [MESH:D003550] (760)  Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478)  Marfan Syndrome [MESH:D008382] (646)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Afibrinogenemia [MESH:D000347] (284)   Afibrinogenemia congenital [MESH:C531603] (280)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 6 [MESH:C563436] (30)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Cornea Plana 2 [MESH:C565677] (9)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Retinitis Pigmentosa [MESH:D012174] (442)   Retinitis Pigmentosa 37 [MESH:C567005] (11)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Hereditary Autoinflammatory Diseases [MESH:D056660] (272)   Periodic fever, familial, autosomal dominant [MESH:C536657] (177)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Metabolism, Inborn Errors [MESH:D008661] (6032)   3-Methylglutaconic Aciduria, Type I [MESH:C562801] (29)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  2-Methylbutyryl-CoA Dehydrogenase Deficiency [MESH:C566487] (38)  Maple Syrup Urine Disease [MESH:D008375] (127)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Peroxisomal Disorders [MESH:D018901] (1472)   Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 1E [MESH:C535743] (16)  Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease XII [MESH:C562718] (98)  Glycogen Storage Disease of Heart, Lethal Congenital [MESH:C564888] (30)  Glycogen Storage Disease 0, Liver [MESH:C565485] (45)  Glycogen Storage Disease Type VI [MESH:D006013] (73)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (365)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Congenital atransferrinemia [MESH:C538259] (145)  Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Gout [MESH:D006073] (261)   Arthritis, Gouty [MESH:D015210] (211)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Fanconi Syndrome [MESH:D005198] (253)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Bile acid synthesis defect, congenital, 1 [MESH:C535442] (25)  Bile acid synthesis defect, congenital, 2 [MESH:C535443] (51)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Meningioma, familial [MESH:C537443] (195)  Juvenile polyposis syndrome [MESH:C537702] (196)  Adenomatous Polyposis Coli [MESH:D011125] (1565)  Hamartoma Syndrome, Multiple [MESH:D006223] (260)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Skin Diseases, Genetic [MESH:D012873] (3456)   Plasminogen Deficiency, Type I [MESH:C566897] (83)  Dermatitis, Atopic [MESH:D003876] (2052)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Asphyxia Neonatorum [MESH:D001238] (1648)  Cystic Fibrosis [MESH:D003550] (760)  Ichthyosis [MESH:D007057] (476)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  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)  Marfan Syndrome [MESH:D008382] (646)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Lipomatosis [MESH:D008068] (182)  Pruritus [MESH:D011537] (647)  Rosacea [MESH:D012393] (32)  Acneiform Eruptions [MESH:D017486] (1312)   Acne Vulgaris [MESH:D000152] (61)  Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Drug Eruptions [MESH:D003875] (2697)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Acne Vulgaris [MESH:D000152] (61)  Chloracne [MESH:D054506] (1274)  Hair Diseases [MESH:D006201] (1891)   Hirsutism [MESH:D006628] (323)  Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)  Keratosis [MESH:D007642] (1941)   Keratosis, Seborrheic [MESH:D017492] (64)  Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)  Sebaceous Gland Diseases [MESH:D012625] (245)   Acne Vulgaris [MESH:D000152] (61)  Skin Abnormalities [MESH:D012868] (1709)   Ichthyosis [MESH:D007057] (481)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Plasminogen Deficiency, Type I [MESH:C566897] (83)  Dermatitis, Atopic [MESH:D003876] (2052)  Sjogren-Larsson Syndrome [MESH:D016111] (67)  Hereditary Autoinflammatory Diseases [MESH:D056660] (247)   Periodic fever, familial, autosomal dominant [MESH:C536657] (177)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Pemphigoid, Bullous [MESH:D010391] (707)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Skin Neoplasms [MESH:D012878] (2991)   Nevus, Epidermal [MESH:C562736] (112) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Acid-Base Imbalance [MESH:D000137] (854)   Acidosis [MESH:D000138] (626)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Peroxisomal Disorders [MESH:D018901] (1472)   Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypocalcemia [MESH:D006996] (378)  Calcinosis [MESH:D002114] (2989)   Nephrocalcinosis [MESH:D009397] (311)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Li-Fraumeni Syndrome [MESH:D016864] (859)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic hypoglycemia, familial, 6 [MESH:C538375] (64)  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)  Hyperinsulinemic hypoglycemia, familial, 6 [MESH:C538375] (64)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Lipomatosis [MESH:D008068] (182)  Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hypertriglyceridemia [MESH:D015228] (808)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (409)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Hypobetalipoproteinemias [MESH:D006995] (181)   Hypobetalipoproteinemia, Familial, Apolipoprotein B [MESH:D052476] (131)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Metabolism, Inborn Errors [MESH:D008661] (6028)   3-Methylglutaconic Aciduria, Type I [MESH:C562801] (29)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  2-Methylbutyryl-CoA Dehydrogenase Deficiency [MESH:C566487] (38)  Maple Syrup Urine Disease [MESH:D008375] (127)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Maple Syrup Urine Disease [MESH:D008375] (127)  MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Leukodystrophy, Metachromatic [MESH:D007966] (76)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Sandhoff Disease [MESH:D012497] (73)  Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Peroxisomal Disorders [MESH:D018901] (1472)   Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Argininosuccinic Aciduria [MESH:D056807] (50)  Ornithine Carbamoyltransferase Deficiency Disease [MESH:D020163] (56)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 1E [MESH:C535743] (16)  Congenital disorder of glycosylation type 2A [MESH:C535752] (38)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease XII [MESH:C562718] (98)  Glycogen Storage Disease of Heart, Lethal Congenital [MESH:C564888] (30)  Glycogen Storage Disease 0, Liver [MESH:C565485] (45)  Glycogen Storage Disease Type VI [MESH:D006013] (73)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)  Medium chain acyl CoA dehydrogenase deficiency [MESH:C536038] (92)  Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemia Type I [MESH:D008072] (219)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hypolipoproteinemias [MESH:D007009] (365)   Hypoalphalipoproteinemias [MESH:D052456] (323)   Familial HDL deficiency [MESH:C538394] (170)  Tangier Disease [MESH:D013631] (170)  Lipidoses [MESH:D008064] (1655)   Sjogren-Larsson Syndrome [MESH:D016111] (67)  Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Gangliosidoses [MESH:D005733] (146)   Gangliosidoses, GM2 [MESH:D020143] (126)   Sandhoff Disease [MESH:D012497] (73)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Congenital atransferrinemia [MESH:C538259] (145)  Hemochromatosis [MESH:D006432] (1694)  Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Zellweger Syndrome [MESH:D015211] (182)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Gout [MESH:D006073] (261)   Arthritis, Gouty [MESH:D015210] (211)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Fanconi Syndrome [MESH:D005198] (253)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Bile acid synthesis defect, congenital, 1 [MESH:C535442] (25)  Bile acid synthesis defect, congenital, 2 [MESH:C535443] (51)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Mitochondrial Diseases [MESH:D028361] (2561)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  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)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Amyloidosis, Familial [MESH:D028226] (696)   Amyloidosis, familial visceral [MESH:C538249] (285)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hyperkalemia [MESH:D006947] (485)  Hypernatremia [MESH:D006955] (215)  Hypocalcemia [MESH:D006996] (368)  Hypokalemia [MESH:D007008] (1041)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin E Deficiency [MESH:D014811] (274)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  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 Cortex Diseases [MESH:D000303] (969)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Adrenal Insufficiency [MESH:D000309] (1599)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Adrenoleukodystrophy [MESH:D000326] (1348)   Peroxisomal ACYL-COA oxidase deficiency [MESH:C536662] (129)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Cushing Syndrome [MESH:D003480] (282)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Thyroid Neoplasms [MESH:D013964] (2040)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  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)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia 2 [MESH:C538236] (89)  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)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)  Pituitary Diseases [MESH:D010900] (1829)   Diabetes Insipidus [MESH:D003919] (302)  Hypopituitarism [MESH:D007018] (732)  Hyperpituitarism [MESH:D006964] (1259)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040)  Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroxinemia [MESH:D006981] (659)   Dystransthyretinemic Euthyroidal Hyperthyroxinemia [MESH:C567719] (136)  Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478) C20. Immune System Diseases  C20. Immune System Diseases  Z. Exceptions (350)   Not Fully Specified [NFS] (350)  Immune System Diseases [MESH:D007154] (7674)   Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Autoimmune Diseases [MESH:D001327] (5067)   Anemia, Hemolytic, Autoimmune [MESH:D000744] (117)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Pemphigoid, Bullous [MESH:D010391] (707)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  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)  Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)   Lupus Nephritis [MESH:D008181] (602)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Anaphylaxis [MESH:D000707] (299)  Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Immune Complex Diseases [MESH:D007105] (782)   Serum Sickness [MESH:D012713] (484)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   Lymphopenia [MESH:D008231] (990)  HIV Infections [MESH:D015658] (3402)   HIV Seropositivity [MESH:D006679] (480)  HIV Wasting Syndrome [MESH:D019247] (1956)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  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)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Paratuberculosis [MESH:D010283] (427)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Calculi [MESH:D002137] (756)   Gallstones [MESH:D042882] (350)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Cysts [MESH:D003560] (133)   Spermatocele [MESH:D013088] (7)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)   Congenital diaphragmatic hernia [MESH:C538080] (381)  Hypertrophy [MESH:D006984] (4476)   Hepatomegaly [MESH:D006529] (1169)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Azotemia [MESH:D053099] (326)  Emphysema [MESH:D004646] (1096)  Hyperammonemia [MESH:D022124] (322)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Leukocytosis [MESH:D007964] (978)  Muscle Weakness [MESH:D018908] (478)  Neointima [MESH:D058426] (814)  Ulcer [MESH:D014456] (392)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Bradycardia [MESH:D001919] (1899)  Long QT Syndrome [MESH:D008133] (691)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Heart Block [MESH:D006327] (571)   Sick Sinus Syndrome [MESH:D012804] (293)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Translocation, Genetic [MESH:D014178] (557)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)  Embryo Loss [MESH:D020964] (288)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Facies [MESH:D019066] (738)   Macrocephaly Autism Syndrome [MESH:C565342] (151)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Hematuria [MESH:D006417] (477)  Shock, Hemorrhagic [MESH:D012771] (2042)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Hyperbilirubinemia [MESH:D006932] (1860)   Jaundice [MESH:D007565] (316)  Inflammation [MESH:D007249] (5241)   Foreign-Body Reaction [MESH:D005549] (6)  Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Oligomenorrhea [MESH:D009839] (228)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)  Necrosis [MESH:D009336] (4019)   Osteonecrosis [MESH:D010020] (537)   Femur Head Necrosis [MESH:D005271] (266)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Pain, Postoperative [MESH:D010149] (529)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Hemorrhagic [MESH:D012771] (2042)  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)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Eye Manifestations [MESH:D005132] (213)   Eye Pain [MESH:D058447] (207)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Ataxia [MESH:D001259] (984)   Ataxia with vitamin E deficiency [MESH:C535393] (271)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Intellectual Disability [MESH:D008607] (1476)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Weakness [MESH:D018908] (478)  Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Facial Paralysis [MESH:D005158] (238)  Gastroparesis [MESH:D018589] (732)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5009)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Vision Disorders [MESH:D014786] (444)   Enhanced S-Cone Syndrome [MESH:C564835] (11)  Diplopia [MESH:D004172] (59)  Pain [MESH:D010146] (4511)   Eye Pain [MESH:D058447] (207)  Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Pain, Postoperative [MESH:D010149] (529)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Constipation [MESH:D003248] (506)  Diarrhea [MESH:D003967] (858)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperoxia [MESH:D018496] (694)  Respiratory Sounds [MESH:D012135] (713)  Skin Manifestations [MESH:D012877] (1250)   Jaundice [MESH:D007565] (316)  Pruritus [MESH:D011537] (648)  Urological Manifestations [MESH:D020924] (3532)   Hypercalciuria [MESH:D053565] (330)  Oliguria [MESH:D009846] (307)  Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)  Virilism [MESH:D014770] (327)   Hirsutism [MESH:D006628] (323) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)   Serum Sickness [MESH:D012713] (484)  Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  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)  Marijuana Abuse [MESH:D002189] (1132)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  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)  Heat Stress Disorders [MESH:D018882] (226)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Foreign Bodies [MESH:D005547] (33)   Foreign-Body Reaction [MESH:D005549] (27)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Rupture [MESH:D012421] (646)   Aortic Rupture [MESH:D001019] (637)  Sprains and Strains [MESH:D013180] (153)   Cumulative Trauma Disorders [MESH:D012090] (151)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Aromatic [MESH:D006841] (19108)   Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (8627)   Naphthacenes [MESH:D009279] (1320)   Tetracyclines [MESH:D013754] (128)   Tetracycline [MESH:D013752] (15) D04. Polycyclic Compounds  D04. Polycyclic Compounds  Polycyclic Compounds [MESH:D011083] (22048)   Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (9200)   Naphthacenes [MESH:D009279] (1320)   Tetracyclines [MESH:D013754] (128)   Tetracycline [MESH:D013752] (15) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Physical Examination [MESH:D010808] (1041)   Body Constitution [MESH:D001824] (450)   Body Weights and Measures [MESH:D001837] (448)   Body Size [MESH:D049628] (439)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Facies [MESH:D019066] (704)   Macrocephaly Autism Syndrome [MESH:C565342] (151) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Mental Disorders [MESH:D001523] (2063)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Cognition Disorders [MESH:D003072] (115)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dementia [MESH:D003704] (471)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Child Development Disorders, Pervasive [MESH:D002659] (157)   Autistic Disorder [MESH:D001321] (154)   Macrocephaly Autism Syndrome [MESH:C565342] (151) G. Phenomena and Processes  G. Phenomena and Processes  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 16-18 [MESH:D002902] (799)   Chromosomes, Human, Pair 17 [MESH:D002886] (779)   Chromosome 17 deletion [MESH:C538045] (769)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Physiological Phenomena [MESH:D010829] (788)   Body Constitution [MESH:D001824] (453)   Body Weights and Measures [MESH:D001837] (444)   Body Size [MESH:D049628] (438)   Body Weight [MESH:D001835] (433)   Overweight [MESH:D050177] (428)   Obesity [MESH:D009765] (427)   Proopiomelanocortin Deficiency [MESH:C565726] (200)