Item 40 of 87 (back to results) previous next   Amitriptyline D000639               MeSH Unique Identifier: D000639 Scope Notes: Tricyclic antidepressant with anticholinergic and sedative properties. It appears to prevent the re-uptake of norepinephrine and serotonin at nerve terminals, thus potentiating the action of these neurotransmitters. Amitriptyline also appears to antagonize cholinergic and alpha-1 adrenergic responses to bioactive amines. Chemical – Gene Interaction Note 1: Amitriptyline results in decreased expression of AP1S1 mRNA Note 2: Amitriptyline results in increased expression of ASAH1 mRNA Click here for more information

Current search: F. Psychiatry and Psychology: Behavior and Behavior Mechanisms [MESH:D001520] > Neurobehavioral Manifestations [MESH:D019954] > Intellectual Disability [MESH:D008607] > Histidinemia [MESH:C538320] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Basic helix-loop-helix [HGNC:BHLH] (618)   sterol regulatory element binding transcription factor 1 [HGNC:SREBF1] (67)  sterol regulatory element binding transcription factor 2 [HGNC:SREBF2] (32)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 01, subfamily A, polypeptide 02 [HGNC:CYP1A2] (466)  cytochrome P450, family 02, subfamily D, polypeptide 06 [HGNC:CYP2D6] (200)  cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612)  cytochrome P450, family 03, subfamily A, polypeptide 05 [HGNC:CYP3A5] (134)  Endogenous Ligands [HGNC:ENDOLIG] (1191)   thyroid stimulating hormone, beta [HGNC:TSHB] (33)  thyrotropin-releasing hormone [HGNC:TRH] (9)  Fatty acid binding protein family [HGNC:FABP] (151)   fatty acid binding protein 1, liver [HGNC:FABP1] (56)  Fatty acid desaturases [HGNC:FADS] (108)   stearoyl-CoA desaturase (delta-9-desaturase) [HGNC:SCD] (78)  Fibronectin type III domain containing [HGNC:FN3] (399)   fibronectin type III domain containing 4 [HGNC:FNDC4] (25)  Glutathione S-transferases [HGNC:GST] (460)   Glutathione S-transferases, soluble [HGNC:SGST] (447)   glutathione S-transferase pi 1 [HGNC:GSTP1] (218)  5-HT (serotonin) receptors [HGNC:HTR] (146)   5-HT (serotonin) receptors, G protein-coupled only [HGNC:HTRGP] (127)   5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled [HGNC:HTR2C] (27)  Nuclear hormone receptors [HGNC:NR] (1322)   nuclear receptor subfamily 0, group B, member 2 [HGNC:NR0B2] (61)  Potassium channels [HGNC:KCN] (298)   Potassium channels, voltage-gated [HGNC:Kv] (224)   potassium voltage-gated channel, subfamily H (eag-related), member 2 [HGNC:KCNH2] (164)  Serine peptidases [HGNC:PRSS] (133)   Serine peptidases, transmembrane [HGNC:TMPRSS] (75)   hepsin [HGNC:HPN] (29)  Solute carriers [HGNC:SLC] (716)   solute carrier family 02 (facilitated glucose transporter), member 03 [HGNC:SLC2A3] (76)  solute carrier family 22 (organic anion transporter), member 06 [HGNC:SLC22A6] (72)  WD repeat domain containing [HGNC:WDR] (199)   WD repeat domain, phosphoinositide interacting 1 [HGNC:WIPI1] (42) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  Decreases (5154)   activity (2549)  expression (2187)  reaction (3393)  Increases (5571)   activity (2865)  cleavage (666)  expression (3238)  metabolic processing (740)  transport (399)  uptake (378) A. Anatomy  A. Anatomy  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Foot Bones [MESH:D005529] (51)   Tarsal Bones [MESH:D013639] (43)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Bones of Upper Extremity [MESH:D001133] (240)   Hand Bones [MESH:D050276] (59)   Carpal Bones [MESH:D002348] (49)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Joints [MESH:D007596] (126)   Hand Joints [MESH:D050823] (57)   Finger Joint [MESH:D005384] (46)   Cushing's symphalangism [MESH:C536223] (42)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Conduction System [MESH:D006329] (263)   Short QT Syndrome 1 [MESH:C566506] (189)  Sense Organs [MESH:D012679] (1060)   Ear [MESH:D004423] (323)   Ear, Middle [MESH:D004432] (49)   Ear Ossicles [MESH:D004429] (40)   Stapes [MESH:D013199] (36)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)  Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   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)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Helminthiasis [MESH:D006373] (1644)   Trematode Infections [MESH:D014201] (1182)   Schistosomiasis [MESH:D012552] (1073)   Schistosomiasis mansoni [MESH:D012555] (1033)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Protozoan Infections [MESH:D011528] (3014)   Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516) 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, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)  Lymphoma [MESH:D008223] (3686)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  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)  Sarcoma [MESH:D012509] (4246)   Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  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)   Neuroendocrine Tumors [MESH:D018358] (3633)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Adenoma, Liver Cell [MESH:D018248] (685)  Mesothelioma [MESH:D008654] (2567)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Small Cell [MESH:D018288] (1317)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Neuroectodermal Tumors [MESH:D017599] (5059)   Neuroendocrine Tumors [MESH:D018358] (3625)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms by Site [MESH:D009371] (9169)   Breast Neoplasms [MESH:D001943] (6077)  Soft Tissue Neoplasms [MESH:D012983] (2003)  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)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)  Head and Neck Neoplasms [MESH:D006258] (4612)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  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)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  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)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Diseases, Developmental [MESH:D001848] (3315)   Osteochondrodysplasias [MESH:D010009] (2440)  Dwarfism [MESH:D004392] (778)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Dysostoses [MESH:D004413] (1019)   Synostosis [MESH:D013580] (817)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Bone Diseases, Endocrine [MESH:D001849] (747)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Joint Diseases [MESH:D007592] (4657)   Cushing's symphalangism [MESH:C536223] (42)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Muscular Diseases [MESH:D009135] (4071)   Muscle Cramp [MESH:D009120] (135)  Muscle Rigidity [MESH:D009127] (617)  Rhabdomyolysis [MESH:D012206] (465)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)  Limb Deformities, Congenital [MESH:D017880] (1813)   Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Synostosis [MESH:D013580] (817)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Rheumatoid [MESH:D001172] (3603) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System 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)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Deglutition Disorders [MESH:D003680] (1538)   Esophageal Motility Disorders [MESH:D015154] (1489)   Gastroesophageal Reflux [MESH:D005764] (1465)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Gastroenteritis [MESH:D005759] (4066)   Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  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)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Intestinal Diseases [MESH:D007410] (6206)   Colonic Diseases [MESH:D003108] (5564)   Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  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)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Drug-Induced Liver Injury [MESH:D056486] (4936)   Drug-Induced Liver Injury, Chronic [MESH:D056487] (14)  Fatty Liver [MESH:D005234] (3584)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis C, Chronic [MESH:D019698] (142)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)   Hepatitis C, Chronic [MESH:D019698] (142)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  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)   Pancreatic Neoplasms [MESH:D010190] (3820)  Pancreatitis [MESH:D010195] (1924) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Oral Ulcer [MESH:D019226] (488)  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)  Salivary Gland Diseases [MESH:D012466] (1213)   Sialorrhea [MESH:D012798] (252)  Xerostomia [MESH:D014987] (98)  Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Respiratory System Abnormalities [MESH:D015619] (243)  Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Laryngeal Diseases [MESH:D007818] (215)   Voice Disorders [MESH:D014832] (52)   Hoarseness [MESH:D006685] (15)  Lung Diseases [MESH:D008171] (7249)   Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Silicosis [MESH:D012829] (1273)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Nose Diseases [MESH:D009668] (1504)   Nasal Obstruction [MESH:D015508] (132)  Rhinitis [MESH:D012220] (1134)  Respiration Disorders [MESH:D012120] (2218)   Dyspnea [MESH:D004417] (248)  Hoarseness [MESH:D006685] (53)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Apnea [MESH:D001049] (748)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Respiratory Insufficiency [MESH:D012131] (841)   Airway Obstruction [MESH:D000402] (191)   Nasal Obstruction [MESH:D015508] (132)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  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) 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)  Tinnitus [MESH:D014012] (109)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Laryngeal Diseases [MESH:D007818] (211)   Voice Disorders [MESH:D014832] (52)   Hoarseness [MESH:D006685] (15)  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)   Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)   Hypotension, Orthostatic [MESH:D007024] (679)  Central Nervous System Diseases [MESH:D002493] (9745)   Ocular Motility Disorders [MESH:D015835] (364)  Brain Diseases [MESH:D001927] (9294)   Cerebellar Diseases [MESH:D002526] (736)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Tourette Syndrome [MESH:D005879] (131)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Kernicterus [MESH:D007647] (256)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Peroxisomal Disorders [MESH:D018901] (1472)   Refsum Disease [MESH:D012035] (173)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsy, Juvenile [MESH:D020190] (166)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Epilepsy, Frontal Lobe [MESH:D017034] (172)   Epilepsy, Nocturnal Frontal Lobe, Type 3 [MESH:C565334] (106)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Absence [MESH:D004832] (222)  Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Tension-Type Headache [MESH:D018781] (8)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Inappropriate ADH Syndrome [MESH:D007177] (178)  Central Nervous System Infections [MESH:D002494] (1823)   Prion Diseases [MESH:D017096] (488)   Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Akathisia, Drug-Induced [MESH:D017109] (75)  Angelman Syndrome [MESH:D017204] (124)  Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Chorea [MESH:D002819] (651)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Essential Tremor [MESH:D020329] (235)   Tremor hereditary essential, 1 [MESH:C536545] (97)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Tic Disorders [MESH:D013981] (256)   Tourette Syndrome [MESH:D005879] (131)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)  Demyelinating Diseases [MESH:D003711] (2917)   Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Neural Tube Defects [MESH:D009436] (2143)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Refsum Disease [MESH:D012035] (173)  Neurodegenerative Diseases [MESH:D019636] (6613)   Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Tourette Syndrome [MESH:D005879] (131)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Refsum Disease [MESH:D012035] (173)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Prion Diseases [MESH:D017096] (475)   Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neurologic Manifestations [MESH:D009461] (8964)   Gait Disorders, Neurologic [MESH:D020233] (491)  Reflex, Abnormal [MESH:D012021] (485)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Ataxia [MESH:D001259] (1138)  Catalepsy [MESH:D002375] (1429)  Chorea [MESH:D002819] (189)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Myoclonus [MESH:D009207] (427)  Psychomotor Agitation [MESH:D011595] (167)  Tremor [MESH:D014202] (840)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Speech Disorders [MESH:D013064] (482)  Confusion [MESH:D003221] (284)   Delirium [MESH:D003693] (173)  Consciousness Disorders [MESH:D003244] (680)   Unconsciousness [MESH:D014474] (660)   Stupor [MESH:D053608] (103)  Syncope [MESH:D013575] (128)  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)   Histidinemia [MESH:C538320] (87)  Brunner Syndrome [MESH:C563156] (124)  Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)  Perceptual Disorders [MESH:D010468] (343)   Hallucinations [MESH:D006212] (251)  Psychomotor Disorders [MESH:D011596] (576)   Psychomotor Agitation [MESH:D011595] (167)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Cramp [MESH:D009120] (135)  Muscle Hypotonia [MESH:D009123] (258)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3875)   Back Pain [MESH:D001416] (287)  Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)  Pupil Disorders [MESH:D011681] (194)   Miosis [MESH:D015877] (106)  Sensation Disorders [MESH:D012678] (5011)   Dizziness [MESH:D004244] (289)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)  Tinnitus [MESH:D014012] (109)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Vision Disorders [MESH:D014786] (501)   Vision, Low [MESH:D015354] (12)  Voice Disorders [MESH:D014832] (52)   Hoarseness [MESH:D006685] (15)  Neuromuscular Diseases [MESH:D009468] (7336)   Muscular Diseases [MESH:D009135] (3538)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Peripheral Nerve Injuries [MESH:D059348] (2)  Radiculopathy [MESH:D011843] (13)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Refsum Disease [MESH:D012035] (173)  Polyradiculoneuropathy [MESH:D011129] (213)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Akathisia, Drug-Induced [MESH:D017109] (75)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Manganese Poisoning [MESH:D020149] (2214)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)  Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)   Cataplexy [MESH:D002385] (20)  Parasomnias [MESH:D020447] (453)   Sleep Arousal Disorders [MESH:D020921] (80)   Somnambulism [MESH:D013009] (75)  Trauma, Nervous System [MESH:D020196] (3997)   Peripheral Nerve Injuries [MESH:D059348] (2)  Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Coma, Post-Head Injury [MESH:D020207] (55) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Ocular Hypertension [MESH:D009798] (1630)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Graves Ophthalmopathy [MESH:D049970] (165)  Eyelid Diseases [MESH:D005141] (882)   Blepharoptosis [MESH:D001763] (117)  Lacrimal Apparatus Diseases [MESH:D007766] (644)   Dry Eye Syndromes [MESH:D015352] (533)  Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Pupil Disorders [MESH:D011681] (230)   Miosis [MESH:D015877] (106)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Degeneration [MESH:D012162] (2386)  Retinal Detachment [MESH:D012163] (1639)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784)  Vision Disorders [MESH:D014786] (534)   Vision, Low [MESH:D015354] (12) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Urogenital Abnormalities [MESH:D014564] (2065)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Hepatorenal Syndrome [MESH:D006530] (910)  Nephrosis [MESH:D009401] (2228)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Pseudohypoaldosteronism [MESH:D011546] (232)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Enuresis [MESH:D004775] (32)  Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)  Urinary Retention [MESH:D016055] (411) 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)  Urogenital Abnormalities [MESH:D014564] (2043)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  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)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Hepatorenal Syndrome [MESH:D006530] (910)  Nephrosis [MESH:D009401] (2228)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Nephritis, Interstitial [MESH:D009395] (1927)  Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)   Pseudohypoaldosteronism [MESH:D011546] (232)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Enuresis [MESH:D004775] (32)  Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)  Urinary Retention [MESH:D016055] (411)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Abruptio Placentae [MESH:D000037] (430)  Placenta Diseases [MESH:D010922] (1781)   Abruptio Placentae [MESH:D000037] (430)  Prenatal Injuries [MESH:D049188] (1314)   Prenatal Exposure Delayed Effects [MESH:D011297] (870) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Short QT Syndrome 1 [MESH:C566506] (189)  Heart Diseases [MESH:D006331] (8614)   Endocarditis [MESH:D004696] (70)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Short QT Syndrome 1 [MESH:C566506] (189)  Bradycardia [MESH:D001919] (1899)  Heart Block [MESH:D006327] (571)   Adams-Stokes Syndrome [MESH:D000219] (11)  Atrioventricular Block [MESH:D054537] (188)  Bundle-Branch Block [MESH:D002037] (45)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 2 [MESH:C563614] (189)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Supraventricular [MESH:D013617] (199)   Tachycardia, Sinus [MESH:D013616] (140)  Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1M [MESH:C564390] (53)  Cardiomyopathies [MESH:D009202] (5331)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Cardiomyopathy, Dilated [MESH:D002311] (1576)   Cardiomyopathy, Dilated, 1M [MESH:C564390] (53)  Heart Arrest [MESH:D006323] (1926)   Death, Sudden, Cardiac [MESH:D016757] (168)  Heart Defects, Congenital [MESH:D006330] (2443)   Short QT Syndrome 1 [MESH:C566506] (189)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Hyperemia [MESH:D006940] (2372)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Thrombosis [MESH:D013927] (3101)   Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypertension [MESH:D006973] (5655)   Hypertension, Essential [MESH:C562386] (1308)  Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy [MESH:C565359] (84)  Hypertension, Malignant [MESH:D006974] (621)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Methemoglobinemia [MESH:D008708] (850)  Anemia [MESH:D000740] (3966)   Anemia, Hypochromic [MESH:D000747] (616)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Kernicterus [MESH:D007647] (256)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)  Blood Protein Disorders [MESH:D001796] (3051)   Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Hemorrhagic Disorders [MESH:D006474] (3359)   Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Leukocyte Disorders [MESH:D007960] (2662)   Eosinophilia [MESH:D004802] (537)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Lymphatic Diseases [MESH:D008206] (5167)   Splenic Diseases [MESH:D013158] (1323)  Lymphoproliferative Disorders [MESH:D008232] (4638)   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)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  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, Drug-Induced [MESH:D000014] (1024)  Respiratory System Abnormalities [MESH:D015619] (244)  Abnormalities, Multiple [MESH:D000015] (3192)   Angelman Syndrome [MESH:D017204] (124)  Down Syndrome [MESH:D004314] (1287)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Short QT Syndrome 1 [MESH:C566506] (189)  Long QT Syndrome [MESH:D008133] (693)   Long Qt Syndrome 2 [MESH:C563614] (189)  Chromosome Disorders [MESH:D025063] (2030)   Angelman Syndrome [MESH:D017204] (124)  Down Syndrome [MESH:D004314] (1287)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)  Limb Deformities, Congenital [MESH:D017880] (1813)   Foot Deformities, Congenital [MESH:D005532] (538)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Hand Deformities, Congenital [MESH:D006228] (587)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Synostosis [MESH:D013580] (817)   NOG-Related-Symphalangism Spectrum Disorder [MESH:C536943] (35)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Neural Tube Defects [MESH:D009436] (2143)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Refsum Disease [MESH:D012035] (173)  Skin Abnormalities [MESH:D012868] (1723)   Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Urogenital Abnormalities [MESH:D014564] (2064)   Hypospadias [MESH:D007021] (798)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  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)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Chromosome Disorders [MESH:D025063] (2030)   Angelman Syndrome [MESH:D017204] (124)  Down Syndrome [MESH:D004314] (1287)  Dwarfism [MESH:D004392] (783)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Brunner Syndrome [MESH:C563156] (124)  Mental Retardation, X-Linked [MESH:D038901] (1867)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hepatolenticular Degeneration [MESH:D006527] (473)  Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Mental Retardation, X-Linked [MESH:D038901] (1848)  Tourette Syndrome [MESH:D005879] (131)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Refsum Disease [MESH:D012035] (173)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Drug Metabolism, Poor, CYP2D6-Related [MESH:C563835] (220)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Gamma aminobutyric acid transaminase deficiency [MESH:C535407] (61)  Histidinemia [MESH:C538320] (87)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Peroxisomal Disorders [MESH:D018901] (1472)   Refsum Disease [MESH:D012035] (173)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Mannosidase Deficiency Diseases [MESH:D044904] (54)   beta-Mannosidosis [MESH:D044905] (23)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Gilbert Disease [MESH:D005878] (259)  Crigler-Najjar Syndrome [MESH:D003414] (255)   Crigler Najjar syndrome, type 2 [MESH:C536213] (254)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Mannosidase Deficiency Diseases [MESH:D044904] (54)   beta-Mannosidosis [MESH:D044905] (23)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Refsum Disease [MESH:D012035] (173)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Pseudohypoaldosteronism [MESH:D011546] (232)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Hyperparathyroidism, Neonatal Severe Primary [MESH:C563375] (50)  Asphyxia Neonatorum [MESH:D001238] (1648)  Erythroblastosis, Fetal [MESH:D004899] (257)   Kernicterus [MESH:D007647] (256)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Ichthyosis [MESH:D007057] (476)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Exanthema [MESH:D005076] (301)  Hair Diseases [MESH:D006201] (1891)  Pruritus [MESH:D011537] (647)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Keratosis [MESH:D007642] (1941)   Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Skin Abnormalities [MESH:D012868] (1709)   Ichthyosis [MESH:D007057] (481)   Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Dermatitis, Atopic [MESH:D003876] (2052)  Ichthyosiform Erythroderma, Congenital [MESH:D016113] (238)   Ichthyosis, Lamellar [MESH:D017490] (81)   Ichthyosiform erythroderma, Brocq congenital, nonbullous form [MESH:C538603] (62)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)  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)   Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Sweat Gland Diseases [MESH:D013543] (231)   Hyperhidrosis [MESH:D006945] (58) 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)  Kernicterus [MESH:D007647] (256)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Peroxisomal Disorders [MESH:D018901] (1472)   Refsum Disease [MESH:D012035] (173)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Hypocalcemia [MESH:D006996] (378)  Hypercalcemia [MESH:D006934] (1999)   Hypocalciuric hypercalcemia, familial, type 1 [MESH:C537145] (50)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Iron Metabolism Disorders [MESH:D019189] (2139)   Anemia, Iron-Deficiency [MESH:D018798] (547)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hypertriglyceridemia [MESH:D015228] (808)  Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Drug Metabolism, Poor, CYP2D6-Related [MESH:C563835] (220)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Gamma aminobutyric acid transaminase deficiency [MESH:C535407] (61)  Histidinemia [MESH:C538320] (87)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Peroxisomal Disorders [MESH:D018901] (1472)   Refsum Disease [MESH:D012035] (173)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Hyperargininemia [MESH:D020162] (109)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Mannosidase Deficiency Diseases [MESH:D044904] (54)   beta-Mannosidosis [MESH:D044905] (23)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Gilbert Disease [MESH:D005878] (259)  Crigler-Najjar Syndrome [MESH:D003414] (255)   Crigler Najjar syndrome, type 2 [MESH:C536213] (254)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Mannosidase Deficiency Diseases [MESH:D044904] (54)   beta-Mannosidosis [MESH:D044905] (23)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hepatolenticular Degeneration [MESH:D006527] (473)  Peroxisomal Disorders [MESH:D018901] (1788)   Acatalasia [MESH:D020642] (788)  Refsum Disease [MESH:D012035] (173)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   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)   Pyruvate Carboxylase Deficiency Disease [MESH:D015324] (55)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Proteostasis Deficiencies [MESH:D057165] (3522)   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)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypocalcemia [MESH:D006996] (368)  Hypokalemia [MESH:D007008] (1041)  Hyponatremia [MESH:D007010] (789)  Inappropriate ADH Syndrome [MESH:D007177] (178)  Hypercalcemia [MESH:D006934] (1999)   Hypocalciuric hypercalcemia, familial, type 1 [MESH:C537145] (50)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin A Deficiency [MESH:D014802] (705)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Dwarfism [MESH:D004392] (698)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)  Gonadal Disorders [MESH:D006058] (5088)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Primary [MESH:D049950] (59)   Hyperparathyroidism, Neonatal Severe Primary [MESH:C563375] (50)  Hypoparathyroidism [MESH:D007011] (376)   Hypoparathyroidism familial isolated [MESH:C537156] (108)  Pituitary Diseases [MESH:D010900] (1829)   Inappropriate ADH Syndrome [MESH:D007177] (178)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Hypothyroidism [MESH:D007037] (496)   Congenital Hypothyroidism [MESH:D003409] (266)   Hypothyroidism, Congenital, Nongoitrous, 4 [MESH:C536917] (105) C20. Immune System Diseases  C20. Immune System Diseases  Z. Exceptions (350)   Not Fully Specified [NFS] (350)  Immune System Diseases [MESH:D007154] (7674)   Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, IGA [MESH:D005922] (897)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Graves Disease [MESH:D006111] (278)   Graves Ophthalmopathy [MESH:D049970] (165)  Blood Group Incompatibility [MESH:D001787] (277)   Erythroblastosis, Fetal [MESH:D004899] (275)   Kernicterus [MESH:D007647] (256)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)  Immune Complex Diseases [MESH:D007105] (782)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   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)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, 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)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Hepatomegaly [MESH:D006529] (1169)  Splenomegaly [MESH:D013163] (1258)  Pathologic Processes [MESH:D010335] (9863)   Ascites [MESH:D001201] (139)  Hemolysis [MESH:D006461] (280)  Ischemia [MESH:D007511] (3049)  Metaplasia [MESH:D008679] (1469)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Short QT Syndrome 1 [MESH:C566506] (189)  Bradycardia [MESH:D001919] (1899)  Heart Block [MESH:D006327] (571)   Adams-Stokes Syndrome [MESH:D000219] (11)  Atrioventricular Block [MESH:D054537] (188)  Bundle-Branch Block [MESH:D002037] (45)  Long QT Syndrome [MESH:D008133] (691)   Long Qt Syndrome 2 [MESH:C563614] (189)  Tachycardia [MESH:D013610] (3339)   Tachycardia, Supraventricular [MESH:D013617] (199)   Tachycardia, Sinus [MESH:D013616] (140)  Tachycardia, Ventricular [MESH:D017180] (1386)   Torsades de Pointes [MESH:D016171] (880)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Translocation, Genetic [MESH:D014178] (557)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)   Death, Sudden, Cardiac [MESH:D016757] (168)  Sudden Infant Death [MESH:D013398] (268)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Growth Disorders [MESH:D006130] (2438)   Fetal Growth Retardation [MESH:D005317] (986)  Hemorrhage [MESH:D006470] (4451)   Hematuria [MESH:D006417] (477)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Hyperbilirubinemia [MESH:D006932] (1860)   Kernicterus [MESH:D007647] (256)  Hyperbilirubinemia, Neonatal [MESH:D051556] (258)   Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254)  Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Inflammation [MESH:D007249] (5241)   Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  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)  Postoperative Complications [MESH:D011183] (5311)   Pain, Postoperative [MESH:D010149] (529)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Signs and Symptoms [MESH:D012816] (10659)   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)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Gait Disorders, Neurologic [MESH:D020233] (491)  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)  Chorea [MESH:D002819] (189)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Myoclonus [MESH:D009207] (263)  Tremor [MESH:D014202] (840)  Psychomotor Agitation [MESH:D011595] (210)   Akathisia, Drug-Induced [MESH:D017109] (75)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Lethargy [MESH:D053609] (1035)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Speech Disorders [MESH:D013064] (482)  Confusion [MESH:D003221] (284)   Delirium [MESH:D003693] (173)  Consciousness Disorders [MESH:D003244] (677)   Unconsciousness [MESH:D014474] (657)   Coma [MESH:D003128] (492)  Stupor [MESH:D053608] (103)  Syncope [MESH:D013575] (128)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Histidinemia [MESH:C538320] (87)  Brunner Syndrome [MESH:C563156] (124)  Perceptual Disorders [MESH:D010468] (343)   Hallucinations [MESH:D006212] (251)  Psychomotor Disorders [MESH:D011596] (576)   Psychomotor Agitation [MESH:D011595] (167)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Cramp [MESH:D009120] (135)  Muscle Hypotonia [MESH:D009123] (258)  Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3869)   Back Pain [MESH:D001416] (285)  Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Ophthalmoplegia [MESH:D009886] (1468)  Pupil Disorders [MESH:D011681] (194)   Miosis [MESH:D015877] (106)  Sensation Disorders [MESH:D012678] (5009)   Dizziness [MESH:D004244] (289)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)  Tinnitus [MESH:D014012] (109)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Paresthesia [MESH:D010292] (416)  Vision Disorders [MESH:D014786] (444)   Vision, Low [MESH:D015354] (12)  Voice Disorders [MESH:D014832] (52)   Hoarseness [MESH:D006685] (15)  Pain [MESH:D010146] (4511)   Abdominal Pain [MESH:D015746] (248)  Back Pain [MESH:D001416] (285)  Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Pain, Postoperative [MESH:D010149] (529)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Abdominal Pain [MESH:D015746] (248)  Anorexia [MESH:D000855] (854)  Constipation [MESH:D003248] (506)  Dyspepsia [MESH:D004415] (59)  Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Dyspnea [MESH:D004417] (248)  Hoarseness [MESH:D006685] (15)  Respiratory Sounds [MESH:D012135] (713)  Apnea [MESH:D001049] (415)   Congenital myasthenic syndrome with episodic apnea [MESH:C535759] (70)  Skin Manifestations [MESH:D012877] (1250)   Pruritus [MESH:D011537] (648)  Jaundice [MESH:D007565] (316)   Jaundice, Obstructive [MESH:D041781] (176)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293) C24. Occupational Diseases  C24. Occupational Diseases  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530)  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Silicosis [MESH:D012829] (1273) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Akathisia, Drug-Induced [MESH:D017109] (75)  Drug Hypersensitivity [MESH:D004342] (4001)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Serotonin Syndrome [MESH:D020230] (49)  Drug-Induced Liver Injury [MESH:D056486] (4936)   Drug-Induced Liver Injury, Chronic [MESH:D056487] (14)  Poisoning [MESH:D011041] (6703)   Manganese Poisoning [MESH:D020149] (2214)  Organophosphate Poisoning [MESH:D062025] (497)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Drug-Induced Liver Injury [MESH:D056486] (4936)   Drug-Induced Liver Injury, Chronic [MESH:D056487] (14)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Akathisia, Drug-Induced [MESH:D017109] (75)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Drug Overdose [MESH:D062787] (513)  Marijuana Abuse [MESH:D002189] (1132)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Tobacco Use Disorder [MESH:D014029] (628)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Opioid-Related Disorders [MESH:D009293] (1491)   Heroin Dependence [MESH:D006556] (950) C26. Wounds and Injuries  C26. Wounds and Injuries  Wounds and Injuries [MESH:D014947] (5171)   Spinal Cord Injuries [MESH:D013119] (2688)  Craniocerebral Trauma [MESH:D006259] (3523)   Coma, Post-Head Injury [MESH:D020207] (55)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Trauma, Nervous System [MESH:D020196] (3535)   Peripheral Nerve Injuries [MESH:D059348] (2)  Craniocerebral Trauma [MESH:D006259] (3507)   Coma, Post-Head Injury [MESH:D020207] (55) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Aromatic [MESH:D006841] (19108)   Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (8627)   Benzocycloheptenes [MESH:D001567] (114)   Dibenzocycloheptenes [MESH:D003986] (92)   Amitriptyline [MESH:D000639] (15) D04. Polycyclic Compounds  D04. Polycyclic Compounds  Polycyclic Compounds [MESH:D011083] (22048)   Polycyclic Hydrocarbons, Aromatic [MESH:D011084] (9200)   Benzocycloheptenes [MESH:D001567] (114)   Dibenzocycloheptenes [MESH:D003986] (92)   Amitriptyline [MESH:D000639] (15) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Behavior [MESH:D001519] (335)   Behavioral Symptoms [MESH:D001526] (173)   Aggression [MESH:D000374] (127)   Brunner Syndrome [MESH:C563156] (124)  Social Behavior [MESH:D012919] (163)   Aggression [MESH:D000374] (125)   Brunner Syndrome [MESH:C563156] (124)  Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Histidinemia [MESH:C538320] (87)  Brunner Syndrome [MESH:C563156] (124)  Mental Disorders [MESH:D001523] (2063)   Impulse Control Disorders [MESH:D007174] (128)   Brunner Syndrome [MESH:C563156] (124)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Histidinemia [MESH:C538320] (87)  Brunner Syndrome [MESH:C563156] (124)