Item 37 of 51 (back to results) previous next   Pentobarbital D010424               MeSH Unique Identifier: D010424 Scope Notes: A short-acting barbiturate that is effective as a sedative and hypnotic (but not as an anti-anxiety) agent and is usually given orally. It is prescribed more frequently for sleep induction than for sedation but, like similar agents, may lose its effectiveness by the second week of continued administration. (From AMA Drug Evaluations Annual, 1994, p236) Chemical – Gene Interaction Note 1: FOLH1 protein results in increased susceptibility to Pentobarbital Note 2: Lindane inhibits the reaction [Pentobarbital promotes the reaction [gamma-Aminobutyric Acid results in increased activity of [GABRA1 protein binds to GABRB3 protein binds to GABRG2 protein]]] Click here for more information

Current search: C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342] > Heredodegenerative Disorders, Nervous System [MESH:D020271] > Neuronal Ceroid-Lipofuscinoses [MESH:D009472] × G. Phenomena and Processes: Musculoskeletal and Neural Physiological Phenomena [MESH:D055687] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Basic leucine zipper proteins [HGNC:bZIP] (670)   jun proto-oncogene [HGNC:JUN] (290)  GABA receptors [HGNC:GABR] (118)   GABA(A) receptors [HGNC:GABRA] (105)   gamma-aminobutyric acid (GABA) A receptor, alpha 1 [HGNC:GABRA1] (57)  gamma-aminobutyric acid (GABA) A receptor, beta 1 [HGNC:GABRB1] (28)  gamma-aminobutyric acid (GABA) A receptor, beta 3 [HGNC:GABRB3] (32)  gamma-aminobutyric acid (GABA) A receptor, gamma 2 [HGNC:GABRG2] (58)  Mitogen-activated protein kinase cascade [HGNC:MAP#K] (854)   Mitogen-activated protein kinases [HGNC:MAPK] (797)   mitogen-activated protein kinase 01 [HGNC:MAPK1] (651)  mitogen-activated protein kinase 03 [HGNC:MAPK3] (644)  Nuclear hormone receptors [HGNC:NR] (1322)   nuclear receptor subfamily 1, group I, member 2 [HGNC:NR1I2] (328)  Potassium channels [HGNC:KCN] (298)   potassium voltage-gated channel, Isk-related family, member 1 [HGNC:KCNE1] (19)  Potassium channels, voltage-gated [HGNC:Kv] (224)   potassium voltage-gated channel, subfamily H (eag-related), member 2 [HGNC:KCNH2] (164)  Solute carriers [HGNC:SLC] (716)   solute carrier family 02 (facilitated glucose transporter), member 01 [HGNC:SLC2A1] (80)  Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898)   tumor necrosis factor [HGNC:TNF] (795) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  cotreatment (1499)  Decreases (5154)   activity (2549)  phosphorylation (590)  reaction (3393)  uptake (71)  Increases (5571)   activity (2865)  expression (3238)  reaction (1574)  response to substance (641)  uptake (378) A. Anatomy  A. Anatomy  Urogenital System [MESH:D014566] (986)   Urinary Tract [MESH:D014551] (721)   Kidney [MESH:D007668] (707)   Nephrons [MESH:D009399] (518)   Kidney Tubules [MESH:D007684] (510)   Kidney Tubules, Proximal [MESH:D007687] (504)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Conduction System [MESH:D006329] (263)   Short QT Syndrome 1 [MESH:C566506] (189)  Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Urinary Tract Infections [MESH:D014552] (984)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Papillomavirus Infections [MESH:D030361] (630)  Herpesviridae Infections [MESH:D006566] (1944)   Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  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)   Cardiovirus Infections [MESH:D018188] (1548)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   HIV Wasting Syndrome [MESH:D019247] (1956)  Tumor Virus Infections [MESH:D014412] (1069)   Papillomavirus Infections [MESH:D030361] (537) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   Nematode Infections [MESH:D009349] (870)   Adenophorea Infections [MESH:D017188] (808)   Enoplida Infections [MESH:D017189] (807)   Trichuriasis [MESH:D014257] (805)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  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)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Aggressive [MESH:D018222] (1562)  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)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (169)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Mesothelioma [MESH:D008654] (2567)  Prolactinoma [MESH:D015175] (312)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Ductal [MESH:D044584] (1786)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  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, Ductal [MESH:D044584] (1786)  Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Gonadal Tissue [MESH:D018309] (284)   Sex Cord-Gonadal Stromal Tumors [MESH:D018312] (282)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  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)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Nevus [MESH:D009506] (340)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neoplasms by Site [MESH:D009371] (9169)   Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Digestive System Neoplasms [MESH:D004067] (7487)   Pancreatic Neoplasms [MESH:D010190] (3820)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)  Thyroid Neoplasms [MESH:D013964] (2040)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Eye Neoplasms [MESH:D005134] (400)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  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)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  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) 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)   Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Osteochondrodysplasias [MESH:D010009] (2440)   Spondyloepimetaphyseal Dysplasia, Missouri Type [MESH:C566574] (142)  Fibrous Dysplasia of Bone [MESH:D005357] (737)   Fibrous Dysplasia, Polyostotic [MESH:D005359] (82)  Osteosclerosis [MESH:D010026] (356)   Osteopetrosis [MESH:D010022] (318)   Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36)  Bone Diseases, Endocrine [MESH:D001849] (747)   Acromegaly [MESH:D000172] (466)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  Bone Resorption [MESH:D001862] (2352)   Alveolar Bone Loss [MESH:D016301] (220)  Osteolysis [MESH:D010014] (1787)   Polyostotic osteolytic dysplasia, hereditary expansile [MESH:C536335] (36)  Osteonecrosis [MESH:D010020] (539)   Femur Head Necrosis [MESH:D005271] (268)  Spinal Diseases [MESH:D013122] (2485)   Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  Joint Diseases [MESH:D007592] (4657)   Synovitis [MESH:D013585] (270)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Psoriatic [MESH:D015535] (1859)  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)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Muscle Rigidity [MESH:D009127] (617)  Muscle Spasticity [MESH:D009128] (187)  Mitochondrial Myopathies [MESH:D017240] (2176)   Mitochondrial Encephalomyopathies [MESH:D017237] (1121)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  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)   Costello Syndrome [MESH:D056685] (407)  Microcephaly [MESH:D008831] (700)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Limb Deformities, Congenital [MESH:D017880] (1813)   Brachydactyly [MESH:D059327] (220)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  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)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Cholelithiasis [MESH:D002769] (373)   Gallstones [MESH:D042882] (350)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Cholecystolithiasis [MESH:D041761] (353)   Gallstones [MESH:D042882] (350)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Digestive System Neoplasms [MESH:D004067] (7493)   Pancreatic Neoplasms [MESH:D010190] (3820)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Gastroenteritis [MESH:D005759] (4066)   Mucositis [MESH:D052016] (1238)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Gastritis [MESH:D005756] (967)   Gastritis, Atrophic [MESH:D005757] (947)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   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)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Fatty Liver [MESH:D005234] (3584)  Hepatomegaly [MESH:D006529] (1169)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis C [MESH:D006526] (1627)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Pancreatic Diseases [MESH:D010182] (4453)   Cystic Fibrosis [MESH:D003550] (760)  Pancreatic Neoplasms [MESH:D010190] (3820)  Pancreatitis [MESH:D010195] (1924) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  PCI 5002 [MESH:C568608] (527)  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)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 10 [MESH:C566605] (39)  PCI 5002 [MESH:C568608] (433)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 10 [MESH:C566605] (39)  PCI 5002 [MESH:C568608] (433)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  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)  Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Periodontal Diseases [MESH:D010510] (1001)   Periodontal Atrophy [MESH:D055093] (225)   Alveolar Bone Loss [MESH:D016301] (220)  Periodontitis [MESH:D010518] (843)   Chronic Periodontitis [MESH:D055113] (231)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 10 [MESH:C566605] (39)  Orofacial Cleft 12 [MESH:C567548] (434)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Tooth Diseases [MESH:D014076] (742)   Toothache [MESH:D014098] (46) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Lung Diseases [MESH:D008171] (7249)   Cystic Fibrosis [MESH:D003550] (760)  Hypertension, Pulmonary [MESH:D006976] (2000)  Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Fibrosis [MESH:D011658] (3140)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Ventilator-Induced Lung Injury [MESH:D055397] (1023)   Bronchopulmonary Dysplasia [MESH:D001997] (1021)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Nose Diseases [MESH:D009668] (1504)   Nasal Obstruction [MESH:D015508] (132)  Rhinitis [MESH:D012220] (1134)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Insufficiency [MESH:D012131] (841)   Respiratory Paralysis [MESH:D012133] (28)  Airway Obstruction [MESH:D000402] (191)   Nasal Obstruction [MESH:D015508] (132)  Hypoventilation [MESH:D007040] (360)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Hearing Loss, Noise-Induced [MESH:D006317] (134)  Nose Diseases [MESH:D009668] (1504)   Nasal Obstruction [MESH:D015508] (132)  Rhinitis [MESH:D012220] (1134) 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)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  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)  Intracranial Hypertension [MESH:D019586] (368)  Basal Ganglia Diseases [MESH:D001480] (4268)   Huntington Disease [MESH:D006816] (540)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  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)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Alexander Disease [MESH:D038261] (168)  Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebellar Diseases [MESH:D002526] (736)   Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 23 [MESH:C537201] (74)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Pituitary Apoplexy [MESH:D010899] (125)  Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Huntington Disease [MESH:D006816] (540)  Lewy Body Disease [MESH:D020961] (1143)  Epilepsy [MESH:D004827] (6274)   Landau-Kleffner Syndrome [MESH:D018887] (87)  Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsy, Juvenile [MESH:D020190] (166)  Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   MERRF Syndrome [MESH:D017243] (1053)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Rolandic [MESH:D019305] (107)  Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Generalized [MESH:D004829] (1431)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Generalized Epilepsy With Febrile Seizures Plus, Type 3 [MESH:C565811] (102)  Epilepsy, Absence [MESH:D004832] (222)  Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Spasms, Infantile [MESH:D013036] (468)  Seizures, Febrile [MESH:D003294] (229)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Generalized Epilepsy With Febrile Seizures Plus, Type 3 [MESH:C565811] (102)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Hypopituitarism [MESH:D007018] (732)  Pituitary Apoplexy [MESH:D010899] (125)  Hyperpituitarism [MESH:D006964] (1250)   Acromegaly [MESH:D000172] (466)  Hyperprolactinemia [MESH:D006966] (603)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Leukoencephalopathies [MESH:D056784] (1916)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Alexander Disease [MESH:D038261] (168)  Central Nervous System Infections [MESH:D002494] (1823)   Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis [MESH:D008581] (1506)   Meningitis, Aseptic [MESH:D008582] (1305)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  Movement Disorders [MESH:D009069] (4823)   Angelman Syndrome [MESH:D017204] (124)  Essential Tremor [MESH:D020329] (235)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)  Dystonic Disorders [MESH:D020821] (729)   Myoclonic dystonia [MESH:C536096] (245)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Ocular Motility Disorders [MESH:D015835] (364)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 23 [MESH:C537201] (74)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Nystagmus, Pathologic [MESH:D009759] (128)  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)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Alexander Disease [MESH:D038261] (168)  Nervous System Malformations [MESH:D009421] (3354)   Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Alexander Disease [MESH:D038261] (168)  Huntington Disease [MESH:D006816] (540)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 23 [MESH:C537201] (74)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Paraneoplastic Syndromes, Nervous System [MESH:D020361] (218)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  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)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Reflex, Abnormal [MESH:D012021] (485)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Ataxia [MESH:D001259] (1138)  Catalepsy [MESH:D002375] (1429)  Hyperkinesis [MESH:D006948] (1799)  Tremor [MESH:D014202] (840)  Myoclonus [MESH:D009207] (427)   Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)  Consciousness Disorders [MESH:D003244] (680)   Unconsciousness [MESH:D014474] (660)   Stupor [MESH:D053608] (103)  Coma [MESH:D003128] (524)   Coma, Post-Head Injury [MESH:D020207] (55)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Mental Retardation, X-Linked [MESH:D038901] (1854)   Fragile X Syndrome [MESH:D005600] (353)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Spasm [MESH:D013035] (418)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Muscle Spasticity [MESH:D009128] (187)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Facial Paralysis [MESH:D005158] (238)  Respiratory Paralysis [MESH:D012133] (28)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Deafness [MESH:D003638] (623)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Hearing Loss, Noise-Induced [MESH:D006317] (134)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Diseases [MESH:D009135] (3538)   Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  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)   Neuralgia [MESH:D009437] (2078)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  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)  Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)  Sleep Apnea Syndromes [MESH:D012891] (570)   Sleep Apnea, Central [MESH:D020182] (347)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  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)  Coma, Post-Head Injury [MESH:D020207] (55) C11. Eye Diseases  C11. Eye Diseases  Z. Exceptions (245)   Not Fully Specified [NFS] (245)  Eye Diseases [MESH:D005128] (6245)   Eye Abnormalities [MESH:D005124] (1233)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Eye Manifestations [MESH:D005132] (208)   Eye Pain [MESH:D058447] (207)  Eye Neoplasms [MESH:D005134] (413)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Ocular Motility Disorders [MESH:D015835] (1699)   Nystagmus, Pathologic [MESH:D009759] (128)  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)   Optic Atrophy [MESH:D009896] (1203)   Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinitis [MESH:D012173] (137)  Retinal Degeneration [MESH:D012162] (2386)   Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Kearns-Sayre Syndrome [MESH:D007625] (1054)  Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Uveal Diseases [MESH:D014603] (2428)   Iris Diseases [MESH:D007499] (348)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Testicular Diseases [MESH:D013733] (451)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Oligospermia [MESH:D009845] (799)   Follicle-stimulating hormone deficiency, isolated [MESH:C537070] (185)  Penile Diseases [MESH:D010409] (1805)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Hyperplasia [MESH:D011470] (336)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Urogenital Abnormalities [MESH:D014564] (2065)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)   Prostate cancer, familial [MESH:C537243] (264)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urologic Diseases [MESH:D014570] (7792)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Diabetes Insipidus [MESH:D003919] (354)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)  Nephrocalcinosis [MESH:D009397] (311)  Nephrosis [MESH:D009401] (2228)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Bartter Syndrome [MESH:D001477] (241)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urinary Bladder Diseases [MESH:D001745] (4374)   Cystitis [MESH:D003556] (604)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Hematuria [MESH:D006417] (477)  Oliguria [MESH:D009846] (307)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Sexual Dysfunction, Physiological [MESH:D012735] (270)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Uterine Diseases [MESH:D014591] (2479)   Uterine Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Urogenital Abnormalities [MESH:D014564] (2043)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Urologic Diseases [MESH:D014570] (7793)   Urinary Tract Infections [MESH:D014552] (984)  Kidney Diseases [MESH:D007674] (7242)   Diabetes Insipidus [MESH:D003919] (354)  Hyperoxaluria [MESH:D006959] (1498)  Hypertension, Renal [MESH:D006977] (698)  Nephrocalcinosis [MESH:D009397] (311)  Nephrosis [MESH:D009401] (2228)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Bartter Syndrome [MESH:D001477] (241)  Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Uremia [MESH:D014511] (2898)   Azotemia [MESH:D053099] (326)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urinary Bladder Diseases [MESH:D001745] (4375)   Cystitis [MESH:D003556] (604)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Hematuria [MESH:D006417] (477)  Oliguria [MESH:D009846] (307)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Placenta Diseases [MESH:D010922] (1781)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Obstetric Labor Complications [MESH:D007744] (1550)   Obstetric Labor, Premature [MESH:D007752] (1316)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870)  Puerperal Disorders [MESH:D011644] (324)   Lactation Disorders [MESH:D007775] (235)   Galactorrhea [MESH:D005687] (233) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Short QT Syndrome 1 [MESH:C566506] (189)  Ductus Arteriosus, Patent [MESH:D004374] (325)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Vascular Malformations [MESH:D054079] (1098)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Heart Diseases [MESH:D006331] (8614)   Cardiac Output, Low [MESH:D002303] (31)  Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Short QT Syndrome 1 [MESH:C566506] (189)  Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial Fibrillation, Familial, 6 [MESH:C567400] (196)  Heart Block [MESH:D006327] (571)   Atrioventricular Block [MESH:D054537] (188)  Sick Sinus Syndrome [MESH:D012804] (293)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 2 [MESH:C563614] (189)  Long Qt Syndrome 5 [MESH:C566766] (40)  Jervell-Lange Nielsen Syndrome [MESH:D029593] (64)  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)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Kearns-Sayre Syndrome [MESH:D007625] (1054)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Short QT Syndrome 1 [MESH:C566506] (189)  Ductus Arteriosus, Patent [MESH:D004374] (325)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Mitral Valve Insufficiency [MESH:D008944] (35)  Pulmonary Valve Insufficiency [MESH:D011665] (9)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Valve, Calcification of [MESH:C562942] (655)  Aortic Stenosis, Subvalvular [MESH:D001020] (203)  Vascular Diseases [MESH:D014652] (8691)   Hyperemia [MESH:D006940] (2372)  Vascular System Injuries [MESH:D057772] (2086)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   MELAS Syndrome [MESH:D017241] (1061)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Pituitary Apoplexy [MESH:D010899] (125)  Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Brain Stem Infarctions [MESH:D020526] (198)   Lateral Medullary Syndrome [MESH:D014854] (188)  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)   Thrombosis [MESH:D013927] (3101)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypertension [MESH:D006973] (5655)   Hypertension, Malignant [MESH:D006974] (621)  Hypertension, Renal [MESH:D006977] (698)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784)  Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Methemoglobinemia [MESH:D008708] (850)  Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Hemolytic [MESH:D000743] (3083)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  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)   Agammaglobulinemia [MESH:D000361] (156)   Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36)  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)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemorrhagic Disorders [MESH:D006474] (3359)   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)  Lymphatic Diseases [MESH:D008206] (5167)   Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Splenic Diseases [MESH:D013158] (1323)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Agammaglobulinemia [MESH:D000361] (156)   Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36)  Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) 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, Multiple [MESH:D000015] (3192)   Angelman Syndrome [MESH:D017204] (124)  Costello Syndrome [MESH:D056685] (407)  Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Short QT Syndrome 1 [MESH:C566506] (189)  Ductus Arteriosus, Patent [MESH:D004374] (325)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 2 [MESH:C563614] (189)  Long Qt Syndrome 5 [MESH:C566766] (40)  Jervell-Lange Nielsen Syndrome [MESH:D029593] (64)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Vascular Malformations [MESH:D054079] (1108)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1018)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Chromosome Disorders [MESH:D025063] (2030)   Angelman Syndrome [MESH:D017204] (124)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Eye Abnormalities [MESH:D005124] (1233)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Microcephaly [MESH:D008831] (700)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Limb Deformities, Congenital [MESH:D017880] (1813)   Brachydactyly [MESH:D059327] (220)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Nervous System Malformations [MESH:D009421] (3354)   Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Malformations of Cortical Development [MESH:D054220] (1406)   Microcephaly [MESH:D008831] (700)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Skin Abnormalities [MESH:D012868] (1723)   Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 10 [MESH:C566605] (39)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 10 [MESH:C566605] (39)  Urogenital Abnormalities [MESH:D014564] (2064)   Allanson Pantzar McLeod syndrome [MESH:C537048] (503)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)  Genetic Diseases, Inborn [MESH:D030342] (9766)   ACTH Deficiency, Isolated [MESH:C562707] (124)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Costello Syndrome [MESH:D056685] (407)  Cystic Fibrosis [MESH:D003550] (760)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Chromosome Disorders [MESH:D025063] (2030)   Angelman Syndrome [MESH:D017204] (124)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Aniridia [MESH:D015783] (312)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Mental Retardation, X-Linked [MESH:D038901] (1867)   Fragile X Syndrome [MESH:D005600] (353)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hereditary Autoinflammatory Diseases [MESH:D056660] (272)   Periodic fever, familial, autosomal dominant [MESH:C536657] (177)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Alexander Disease [MESH:D038261] (168)  Huntington Disease [MESH:D006816] (540)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth disease, X-linked, 1 [MESH:C535919] (72)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Fragile X Syndrome [MESH:D005600] (353)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Optic Atrophies, Hereditary [MESH:D015418] (1151)   Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia 23 [MESH:C537201] (74)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Myeloperoxidase Deficiency [MESH:C562864] (335)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Hyperhomocysteinemia [MESH:D020138] (1724)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Alexander Disease [MESH:D038261] (168)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)   Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Adenomatous Polyposis Coli [MESH:D011125] (1565)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Wilms Tumor [MESH:D009396] (553)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Skin Diseases, Genetic [MESH:D012873] (3456)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Dermatitis, Atopic [MESH:D003876] (2052)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Cystic Fibrosis [MESH:D003550] (760)  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)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Scleroderma, Localized [MESH:D012594] (1597)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Keratosis [MESH:D007642] (1941)  Scleroderma, Localized [MESH:D012594] (1597)  Skin Neoplasms [MESH:D012878] (2991)  Breast Diseases [MESH:D001941] (6148)   Gynecomastia [MESH:D006177] (484)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Lactation Disorders [MESH:D007775] (235)   Galactorrhea [MESH:D005687] (233)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Drug Eruptions [MESH:D003875] (2697)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hair Diseases [MESH:D006201] (1891)   Hirsutism [MESH:D006628] (323)  Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)  Pigmentation Disorders [MESH:D010859] (1215)   Cafe-au-Lait Spots [MESH:D019080] (186)  Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Skin Abnormalities [MESH:D012868] (1709)   Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  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)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Dermatitis, Atopic [MESH:D003876] (2052)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Hereditary Autoinflammatory Diseases [MESH:D056660] (247)   Periodic fever, familial, autosomal dominant [MESH:C536657] (177)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158)  Urticaria [MESH:D014581] (2668) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Metabolic Syndrome X [MESH:D024821] (2151)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Alexander Disease [MESH:D038261] (168)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Hypercalcemia [MESH:D006934] (1999)  Hypocalcemia [MESH:D006996] (378)  Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  Nephrocalcinosis [MESH:D009397] (311)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Fanconi Anemia [MESH:D005199] (1604)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   ACTH Deficiency, Isolated [MESH:C562707] (124)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypercholesterolemia [MESH:D006937] (1404)  Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Myeloperoxidase Deficiency [MESH:C562864] (335)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Hyperhomocysteinemia [MESH:D020138] (1724)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   MELAS Syndrome [MESH:D017241] (1061)  MERRF Syndrome [MESH:D017243] (1053)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Alexander Disease [MESH:D038261] (168)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   De Vivo disease [MESH:C536830] (172)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Pseudohypoparathyroidism [MESH:D011547] (88)   Albright's hereditary osteodystrophy [MESH:C537045] (82)  Pseudohypoparathyroidism Type 1B [MESH:C548075] (82)  Pseudopseudohypoparathyroidism [MESH:D011556] (82)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  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)   Liddle Syndrome [MESH:D056929] (200)  Pseudohypoaldosteronism [MESH:D011546] (232)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Mitochondrial Diseases [MESH:D028361] (2561)   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)  Phosphorus Metabolism Disorders [MESH:D010760] (711)   Hypophosphatemia [MESH:D017674] (640)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  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)   Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Obesity, Morbid [MESH:D009767] (515)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Z. Exceptions (123)   Not Fully Specified [NFS] (123)  Endocrine System Diseases [MESH:D004700] (8062)   ACTH Deficiency, Isolated [MESH:C562707] (124)  Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)  Adrenal Gland Neoplasms [MESH:D000310] (917)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Adrenal Insufficiency [MESH:D000309] (1599)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Adrenocortical Hyperfunction [MESH:D000308] (618)   Cushing Syndrome [MESH:D003480] (282)  Hyperaldosteronism [MESH:D006929] (419)   Bartter Syndrome [MESH:D001477] (241)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Adrenal Gland Neoplasms [MESH:D000310] (917)  Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)  Thyroid Neoplasms [MESH:D013964] (2040)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Delayed [MESH:D011628] (449)  Puberty, Precocious [MESH:D011629] (1147)  Disorders of Sex Development [MESH:D012734] (1637)   46, XY Disorders of Sex Development [MESH:D058490] (1060)   WAGR Syndrome [MESH:D017624] (270)   Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Hypogonadism [MESH:D007006] (1123)   Eunuchism [MESH:D005058] (51)   Fertile eunuch syndrome [MESH:C537919] (49)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Testicular Neoplasms [MESH:D013736] (520)   Sertoli-Leydig Cell Tumor [MESH:D018310] (272)   Leydig Cell Tumor [MESH:D007984] (267)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Pituitary Diseases [MESH:D010900] (1829)   Diabetes Insipidus [MESH:D003919] (302)  Hypopituitarism [MESH:D007018] (732)  Pituitary Apoplexy [MESH:D010899] (125)  Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Hyperprolactinemia [MESH:D006966] (603)  Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Pituitary Neoplasms [MESH:D010911] (981)   ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172)  Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383)  Prolactinoma [MESH:D015175] (312)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040) C20. Immune System Diseases  C20. Immune System Diseases  Z. Exceptions (350)   Not Fully Specified [NFS] (350)  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Glomerulonephritis, IGA [MESH:D005922] (897)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Urticaria [MESH:D014581] (2668)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   MYD88 Deficiency [MESH:C567379] (79)  Lymphopenia [MESH:D008231] (990)  Agammaglobulinemia [MESH:D000361] (156)   Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36)  HIV Infections [MESH:D015658] (3402)   HIV Wasting Syndrome [MESH:D019247] (1956)  AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Plaque, Amyloid [MESH:D058225] (334)  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)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Hypertrophy [MESH:D006984] (4476)   Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  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)  Fibrosis [MESH:D005355] (3133)  Gliosis [MESH:D005911] (1419)  Hyperbilirubinemia [MESH:D006932] (1860)  Hyperplasia [MESH:D006965] (2463)  Leukocytosis [MESH:D007964] (978)  Metaplasia [MESH:D008679] (1469)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Short QT Syndrome 1 [MESH:C566506] (189)  Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Arrhythmia, Sinus [MESH:D001146] (324)   Sick Sinus Syndrome [MESH:D012804] (293)  Atrial Fibrillation [MESH:D001281] (1053)   Atrial Fibrillation, Familial, 6 [MESH:C567400] (196)  Heart Block [MESH:D006327] (571)   Atrioventricular Block [MESH:D054537] (188)  Sick Sinus Syndrome [MESH:D012804] (293)  Long QT Syndrome [MESH:D008133] (691)   Long Qt Syndrome 2 [MESH:C563614] (189)  Long Qt Syndrome 5 [MESH:C566766] (40)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Death [MESH:D003643] (1328)   Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  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)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Ischemia [MESH:D007511] (3049)   Infarction [MESH:D007238] (298)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Necrosis [MESH:D009336] (4019)   Infarction [MESH:D007238] (298)  Osteonecrosis [MESH:D010020] (537)   Femur Head Necrosis [MESH:D005271] (266)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Ossification, Heterotopic [MESH:D009999] (187)   Osseous Heteroplasia, Progressive [MESH:C562735] (82)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Cardiac Output, Low [MESH:D002303] (31)  Edema [MESH:D004487] (3726)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)   Proopiomelanocortin Deficiency [MESH:C565726] (200)  Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Obesity, Morbid [MESH:D009767] (515)  Eye Manifestations [MESH:D005132] (213)   Eye Pain [MESH:D058447] (207)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Neurologic Manifestations [MESH:D009461] (8702)   Reflex, Abnormal [MESH:D012021] (485)  Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Ataxia [MESH:D001259] (984)  Catalepsy [MESH:D002375] (1429)  Hyperkinesis [MESH:D006948] (1799)  Myoclonus [MESH:D009207] (263)  Tremor [MESH:D014202] (840)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Intellectual Disability [MESH:D008607] (1476)  Psychomotor Disorders [MESH:D011596] (576)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)  Consciousness Disorders [MESH:D003244] (677)   Unconsciousness [MESH:D014474] (657)   Coma [MESH:D003128] (492)  Stupor [MESH:D053608] (103)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Spasm [MESH:D013035] (418)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Muscle Spasticity [MESH:D009128] (187)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Facial Paralysis [MESH:D005158] (238)  Respiratory Paralysis [MESH:D012133] (28)  Ophthalmoplegia [MESH:D009886] (1468)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Deafness [MESH:D003638] (593)  Hearing Loss, Sensorineural [MESH:D006319] (1227)   Hearing Loss, Noise-Induced [MESH:D006317] (134)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Eye Pain [MESH:D058447] (207)  Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Facial Pain [MESH:D005157] (56)   Toothache [MESH:D014098] (46)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Constipation [MESH:D003248] (506)  Hiccup [MESH:D006606] (49)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hypercapnia [MESH:D006935] (264)  Hyperoxia [MESH:D018496] (694)  Hypoventilation [MESH:D007040] (359)   Congenital central hypoventilation syndrome [MESH:C536209] (341)  Skin Manifestations [MESH:D012877] (1250)   Cafe-au-Lait Spots [MESH:D019080] (186)  Urological Manifestations [MESH:D020924] (3532)   Hypercalciuria [MESH:D053565] (330)  Oliguria [MESH:D009846] (307)  Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Virilism [MESH:D014770] (327)   Hirsutism [MESH:D006628] (323) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  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)  Tobacco Use Disorder [MESH:D014029] (628)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950)  Morphine Dependence [MESH:D009021] (855) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Coma, Post-Head Injury [MESH:D020207] (55)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Thoracic Injuries [MESH:D013898] (1831)   Lung Injury [MESH:D055370] (1814)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431)  Coma, Post-Head Injury [MESH:D020207] (55) D03. Heterocyclic Compounds  D03. Heterocyclic Compounds  Heterocyclic Compounds [MESH:D006571] (56330)   Heterocyclic Compounds, 1-Ring [MESH:D006573] (30631)   Pyrimidines [MESH:D011743] (4670)   Pyrimidinones [MESH:D011744] (1346)   Barbiturates [MESH:D001463] (233)   Pentobarbital [MESH:D010424] (10) 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)  Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407) G. Phenomena and Processes  G. Phenomena and Processes  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)  Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)  Musculoskeletal and Neural Physiological Phenomena [MESH:D055687] (260)   Musculoskeletal Physiological Phenomena [MESH:D009142] (128)   Musculoskeletal Physiological Processes [MESH:D043702] (107)   Bone Remodeling [MESH:D016723] (50)   Bone Resorption [MESH:D001862] (47)   Osteolysis [MESH:D010014] (46)   Polyostotic osteolytic dysplasia, hereditary expansile [MESH:C536335] (36)