Item 29 of 41 (back to results) previous next   Piperonyl Butoxide D010882               MeSH Unique Identifier: D010882 Scope Notes: An insecticide synergist, especially for pyrethroids and ROTENONE. Chemical – Gene Interaction Note 1: Piperonyl Butoxide results in increased expression of CYP1A1 mRNA Note 2: Piperonyl Butoxide results in increased expression of CYP1A1 protein Click here for more information

Current search: C02. Virus Diseases: Virus Diseases [MESH:D014777] > Viremia [MESH:D014766] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566)  cytochrome P450, family 01, subfamily A, polypeptide 02 [HGNC:CYP1A2] (466)  Interferons and interferon receptors [HGNC:IFN] (684)   interferon, gamma [HGNC:IFNG] (274)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 04 [HGNC:IL4] (164)  OTU domain containing [HGNC:OTUD] (88)   tumor necrosis factor, alpha-induced protein 3 [HGNC:TNFAIP3] (88) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   cotreatment (1499)  Decreases (5154)   expression (2187)  Increases (5571)   expression (3238) 4. Semantic Terms  4. Semantic Terms  Entity [STY:T071] (48056)   Physical Object [STY:T072] (47583)   Substance [STY:T167] (46174)   Chemical [STY:T103] (46110)   Chemical Viewed Functionally [STY:T120] (28747)   Hazardous or Poisonous Substance [STY:T131] (590)  Pharmacologic Substance [STY:T121] (11019)  Chemical Viewed Structurally [STY:T104] (44741)   Organic Chemical [STY:T109] (44144) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Syndactyly, type 3 [MESH:C538154] (192)  Sense Organs [MESH:D012679] (1060)   Eye [MESH:D005123] (858)   Anterior Eye Segment [MESH:D000869] (664)   Peters anomaly [MESH:C537884] (465)  Stomatognathic System [MESH:D013284] (673)   Mouth [MESH:D009055] (194)   Dentition [MESH:D003817] (109)   Tooth [MESH:D014070] (61)   Incisor [MESH:D007180] (51)   Single upper central incisor [MESH:C537342] (50) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Enterobacteriaceae Infections [MESH:D004756] (669)   Salmonella Infections [MESH:D012480] (620)   Salmonella Infections, Animal [MESH:D012481] (604)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Staphylococcal Infections [MESH:D013203] (264)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Tuberculosis [MESH:D014376] (992)   Tuberculosis, Bovine [MESH:D014380] (380)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Intraabdominal Infections [MESH:D059413] (958)   Appendicitis [MESH:D001064] (774)  Peritonitis [MESH:D010538] (800)  Sepsis [MESH:D018805] (3556)   Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   Viremia [MESH:D014766] (41)  Central Nervous System Viral Diseases [MESH:D020805] (1416)   Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)  Herpesviridae Infections [MESH:D006566] (1944)   Sarcoma, Kaposi [MESH:D012514] (1578)  Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)  Meningitis, Viral [MESH:D008587] (1308)   Meningitis, Aseptic [MESH:D008582] (1305)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Slow Virus Diseases [MESH:D012897] (782)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  Tumor Virus Infections [MESH:D014412] (1069)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Helminthiasis [MESH:D006373] (1644)   Nematode Infections [MESH:D009349] (870)   Adenophorea Infections [MESH:D017188] (808)   Enoplida Infections [MESH:D017189] (807)   Trichuriasis [MESH:D014257] (805)  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, Visceral [MESH:D007898] (2149)  Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Neoplasms, Second Primary [MESH:D016609] (518)  Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Hamartoma [MESH:D006222] (1484)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  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, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Hepatoblastoma [MESH:D018197] (548)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Adipose Tissue [MESH:D018205] (677)   Liposarcoma [MESH:D008080] (612)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Liposarcoma [MESH:D008080] (612)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Kaposi [MESH:D012514] (1578)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Mesothelioma [MESH:D008654] (2567)  Carcinoma [MESH:D002277] (7263)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Lewis Lung [MESH:D018827] (248)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   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, Pancreatic Ductal [MESH:D021441] (1056)  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)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Meningioma [MESH:D008579] (978)  Sarcoma, Kaposi [MESH:D012514] (1578)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Skin Neoplasms [MESH:D012878] (2992)  Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  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)   Colonic Neoplasms [MESH:D003110] (4405)  Rectal Neoplasms [MESH:D012004] (717)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Eye Neoplasms [MESH:D005134] (400)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  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)  Tongue Neoplasms [MESH:D014062] (1518)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Carcinoma, Lewis Lung [MESH:D018827] (248)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Tuberous Sclerosis [MESH:D014402] (635)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  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 Resorption [MESH:D001862] (2352)  Bone Diseases, Developmental [MESH:D001848] (3315)   Dwarfism [MESH:D004392] (778)   Laron Syndrome [MESH:D046150] (91)  Dwarfism, Pituitary [MESH:D004393] (235)   Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Dysostoses [MESH:D004413] (1019)   Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Osteochondrodysplasias [MESH:D010009] (2440)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Fibrous Dysplasia of Bone [MESH:D005357] (737)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Bone Diseases, Endocrine [MESH:D001849] (747)   Dwarfism, Pituitary [MESH:D004393] (235)   Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Hyperostosis [MESH:D015576] (493)   Exostoses [MESH:D005096] (160)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Foot Deformities [MESH:D005530] (553)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Muscular Diseases [MESH:D009135] (4071)   Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Mitochondrial Myopathies [MESH:D017240] (2176)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2071)   Polymyositis [MESH:D017285] (2007)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Limb Deformities, Congenital [MESH:D017880] (1813)   Lower Extremity Deformities, Congenital [MESH:D038061] (560)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Bile Duct Neoplasms [MESH:D001650] (367)  Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Bile Duct Neoplasms [MESH:D001650] (367)  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)  Rectal Neoplasms [MESH:D012004] (717)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Deglutition Disorders [MESH:D003680] (1538)   Esophageal Motility Disorders [MESH:D015154] (1489)   Esophageal Achalasia [MESH:D004931] (29)   Achalasia Addisonianism Alacrimia syndrome [MESH:C536008] (24)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Gastroenteritis [MESH:D005759] (4066)   Appendicitis [MESH:D001064] (774)  Colitis [MESH:D003092] (3199)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   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)  Rectal Neoplasms [MESH:D012004] (717)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Appendicitis [MESH:D001064] (774)  Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   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)  Rectal Neoplasms [MESH:D012004] (717)  Malabsorption Syndromes [MESH:D008286] (492)   Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Rectal Neoplasms [MESH:D012004] (717)  Peptic Ulcer [MESH:D010437] (3172)   Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)  Liver Cirrhosis [MESH:D008103] (5542)   Cirrhosis, Familial [MESH:C566123] (179)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   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)   Pancreatitis [MESH:D010195] (1924)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Peritoneal Diseases [MESH:D010532] (1119)   Peritonitis [MESH:D010538] (800) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation [MESH:C566509] (71)  Cleft Palate [MESH:D002972] (1330)   PCI 5002 [MESH:C568608] (527)  Mouth Diseases [MESH:D009059] (4783)   Oral Submucous Fibrosis [MESH:D009914] (2432)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   PCI 5002 [MESH:C568608] (433)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   PCI 5002 [MESH:C568608] (433)  Cleft Palate [MESH:D002972] (1330)   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)   Periodontitis [MESH:D010518] (843)   Periodontitis, Aggressive, 2 [MESH:C566946] (310)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)   Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia [MESH:C538340] (365)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation [MESH:C566509] (71)  Cleft Palate [MESH:D002972] (1330)   Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 12 [MESH:C567548] (434)  Cleft Palate [MESH:D002972] (1330)   Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50) 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)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Lung Diseases [MESH:D008171] (7249)   Pneumonia [MESH:D011014] (3482)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Berylliosis [MESH:D001607] (2005)  Silicosis [MESH:D012829] (1273)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Pneumoconiosis [MESH:D011009] (2789)   Berylliosis [MESH:D001607] (2005)  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)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Nose Diseases [MESH:D009668] (1504)   Paranasal Sinus Diseases [MESH:D010254] (476)   Sinusitis [MESH:D012852] (469)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiration Disorders [MESH:D012120] (2218)   Hyperventilation [MESH:D006985] (654)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Sinusitis [MESH:D012852] (469)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  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)  Labyrinth Diseases [MESH:D007759] (846)   Vestibular Diseases [MESH:D015837] (819)  Nose Diseases [MESH:D009668] (1504)   Paranasal Sinus Diseases [MESH:D010254] (476)   Sinusitis [MESH:D012852] (469)  Rhinitis [MESH:D012220] (1134)   Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Chronobiology Disorders [MESH:D021081] (970)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Brain Neoplasms [MESH:D001932] (2764)  Basal Ganglia Diseases [MESH:D001480] (4268)   Huntington Disease [MESH:D006816] (540)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Tyrosinemias [MESH:D020176] (132)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Glycogen Storage Disease Type II [MESH:D006009] (37)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  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)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   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)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Huntington Disease [MESH:D006816] (540)  Epilepsy [MESH:D004827] (6274)   Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Myoclonic Epilepsies, Progressive [MESH:D020191] (1101)   Unverricht-Lundborg Syndrome [MESH:D020194] (65)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  Seizures [MESH:D012640] (4502)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Hypothalamic Diseases [MESH:D007027] (1833)   Pituitary Diseases [MESH:D010900] (1808)   Hypopituitarism [MESH:D007018] (732)   Dwarfism, Pituitary [MESH:D004393] (235)   Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Adrenoleukodystrophy [MESH:D000326] (1348)  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)   Dyskinesias [MESH:D020820] (1827)   Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Adrenoleukodystrophy [MESH:D000326] (1348)  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)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive [MESH:C564948] (44)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Malformations of Cortical Development [MESH:D054220] (1406)   Tuberous Sclerosis [MESH:D014402] (635)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Tuberous Sclerosis [MESH:D014402] (635)  von Hippel-Lindau Disease [MESH:D006623] (580)  Neurodegenerative Diseases [MESH:D019636] (6613)   Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Huntington Disease [MESH:D006816] (540)  Tuberous Sclerosis [MESH:D014402] (635)  Unverricht-Lundborg Syndrome [MESH:D020194] (65)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive [MESH:C564948] (44)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Paralysis [MESH:D010243] (2043)  Dyskinesias [MESH:D020820] (3365)   Hyperkinesis [MESH:D006948] (1799)  Tremor [MESH:D014202] (840)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Histidinemia [MESH:C538320] (87)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Seizures [MESH:D012640] (4514)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)  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)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Diseases [MESH:D009135] (3538)   Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Mitochondrial Myopathies [MESH:D017240] (2176)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myositis [MESH:D009220] (2069)   Polymyositis [MESH:D017285] (2007)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive [MESH:C564948] (44)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Polyradiculoneuropathy [MESH:D011129] (213)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eyelid Diseases [MESH:D005141] (882)  Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Corneal Opacity [MESH:D003318] (544)   Peters anomaly [MESH:C537884] (465)  Eye Abnormalities [MESH:D005124] (1233)   Peters anomaly [MESH:C537884] (465)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Coloboma [MESH:D003103] (315)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Eye Neoplasms [MESH:D005134] (413)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Ocular Hypertension [MESH:D009798] (1630)   Glaucoma [MESH:D005901] (1458)   Glaucoma 3, Primary Congenital, A [MESH:C565547] (434)  Glaucoma, Open-Angle [MESH:D005902] (1281)   Glaucoma, Primary Open Angle [MESH:C562750] (466)  Glaucoma 1, Open Angle, A [MESH:C564234] (446)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Edema [MESH:D008269] (557)  Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157)  Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550) 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)   Oligospermia [MESH:D009845] (799)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  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)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  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)   Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  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)   Hypomagnesemia 4, Renal [MESH:C567127] (225)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  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)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urogenital Abnormalities [MESH:D014564] (2043)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urologic Neoplasms [MESH:D014571] (5315)   Ureteral Neoplasms [MESH:D014516] (574)  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)   Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  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)   Hypomagnesemia 4, Renal [MESH:C567127] (225)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Ureteral Diseases [MESH:D014515] (1024)   Ureteral Neoplasms [MESH:D014516] (574)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Cystitis [MESH:D003556] (604)   Cystitis, Interstitial [MESH:D018856] (264)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Abruptio Placentae [MESH:D000037] (430)  Obstetric Labor, Premature [MESH:D007752] (1316)  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  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  Vascular Malformations [MESH:D054079] (1098)   Arteriovenous Malformations [MESH:D001165] (1058)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Heart Diseases [MESH:D006331] (8614)   Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Tachycardia [MESH:D013610] (3339)  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)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Heart Defects, Congenital [MESH:D006330] (2443)   Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Insufficiency [MESH:D001022] (1002)  Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Ventricular Dysfunction [MESH:D018754] (2348)   Ventricular Dysfunction, Left [MESH:D018487] (1631)  Vascular Diseases [MESH:D014652] (8691)   Arteritis [MESH:D001167] (1084)  Hypotension [MESH:D007022] (4045)  Retinal Vein Occlusion [MESH:D012170] (607)  Varicose Veins [MESH:D014648] (383)  Vascular System Injuries [MESH:D057772] (2086)  Aneurysm [MESH:D000783] (1886)   Coronary Aneurysm [MESH:D003323] (204)  Angiomatosis [MESH:D000798] (620)   von Hippel-Lindau Disease [MESH:D006623] (580)  Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  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)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   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)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  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)   Thromboembolism [MESH:D013923] (732)  Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Thrombosis [MESH:D013927] (3101)   Thromboembolism [MESH:D013923] (732)  Venous Thrombosis [MESH:D020246] (1141)   Retinal Vein Occlusion [MESH:D012170] (607)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Hypertension [MESH:D006973] (5655)   Hypertension, Malignant [MESH:D006974] (621)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Aneurysm [MESH:D003323] (204)  Coronary Artery Disease [MESH:D003324] (2685)  Peripheral Vascular Diseases [MESH:D016491] (1412)   Raynaud Disease [MESH:D011928] (490)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Adenosine Triphosphate, Elevated, Of Erythrocytes [MESH:C566310] (78)  Blood Coagulation Disorders [MESH:D001778] (1828)  Methemoglobinemia [MESH:D008708] (850)  Anemia [MESH:D000740] (3966)   Anemia, Sideroblastic [MESH:D000756] (636)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Diamond-Blackfan Anemia 8 [MESH:C567253] (45)  Anemia, Hemolytic [MESH:D000743] (3083)   Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to [MESH:C565545] (88)  Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to [MESH:C565557] (312)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Red-Cell Aplasia, Pure [MESH:D012010] (183)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Diamond-Blackfan Anemia 8 [MESH:C567253] (45)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Blood Protein Disorders [MESH:D001796] (3051)   Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Diamond-Blackfan Anemia 8 [MESH:C567253] (45)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Sideroblastic [MESH:D000756] (636)  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)   Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)  Lymphatic Diseases [MESH:D008206] (5167)   Splenic Diseases [MESH:D013158] (1323)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  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, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  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)  Abnormalities, Multiple [MESH:D000015] (3192)   Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Coronary Vessel Anomalies [MESH:D003330] (317)  Hypoplastic Left Heart Syndrome [MESH:D018636] (194)  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)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Eye Abnormalities [MESH:D005124] (1233)   Peters anomaly [MESH:C537884] (465)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Coloboma [MESH:D003103] (315)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Microphthalmos [MESH:D008850] (273)   Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Craniofacial Dysostosis [MESH:D003394] (391)   Hallermann's Syndrome [MESH:D006210] (193)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Limb Deformities, Congenital [MESH:D017880] (1813)   Foot Deformities, Congenital [MESH:D005532] (538)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Synostosis [MESH:D013580] (817)   Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Syndactyly [MESH:D013576] (487)   Syndactyly, type 3 [MESH:C538154] (192)  Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Nervous System Malformations [MESH:D009421] (3354)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Neural Tube Defects [MESH:D009436] (2143)  Agenesis of Corpus Callosum [MESH:D061085] (345)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Central Nervous System Vascular Malformations [MESH:D020785] (1031)   Intracranial Arteriovenous Malformations [MESH:D002538] (1015)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive [MESH:C564948] (44)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Malformations of Cortical Development [MESH:D054220] (1406)   Tuberous Sclerosis [MESH:D014402] (635)  Microcephaly [MESH:D008831] (700)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Skin Abnormalities [MESH:D012868] (1723)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Cleft Palate [MESH:D002972] (1330)  Tooth Abnormalities [MESH:D014071] (622)   Oculodentodigital Dysplasia [MESH:C563160] (192)  Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)  Anodontia [MESH:D000848] (185)   Single upper central incisor [MESH:C537342] (50)  Urogenital Abnormalities [MESH:D014564] (2064)   Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Hypospadias [MESH:D007021] (798)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Platelet Glycoprotein IV Deficiency [MESH:C564245] (173)  Cirrhosis, Familial [MESH:C566123] (179)  Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Anemia, Diamond-Blackfan [MESH:D029503] (158)   Anemia, Diamond-Blackfan, 3 [MESH:C536355] (35)  Diamond-Blackfan Anemia 8 [MESH:C567253] (45)  Chromosome Disorders [MESH:D025063] (2030)   Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 3 [MESH:C564181] (50)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Dwarfism [MESH:D004392] (783)   Laron Syndrome [MESH:D046150] (91)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Hypospadias 1, X-Linked [MESH:C567482] (571)  Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Bulbo-Spinal Atrophy, X-Linked [MESH:D055534] (566)   Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Huntington Disease [MESH:D006816] (540)  Tuberous Sclerosis [MESH:D014402] (635)  Unverricht-Lundborg Syndrome [MESH:D020194] (65)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive [MESH:C564948] (44)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia, Autosomal Recessive 9 [MESH:C567436] (49)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Xanthinuria, Type I [MESH:C562584] (190)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutamine deficiency, congenital [MESH:C536832] (117)  Glutathione synthetase deficiency [MESH:C536835] (88)  Glutathionuria [MESH:C536836] (96)  Histidinemia [MESH:C538320] (87)  Hyperprolinemia [MESH:C538384] (45)  Methionine Adenosyltransferase Deficiency [MESH:C562681] (56)  Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  Glycine N-Methyltransferase Deficiency [MESH:C564683] (72)  Dimethylglycine Dehydrogenase Deficiency [MESH:C565278] (33)  Hyperhomocysteinemia [MESH:D020138] (1724)  Tyrosinemias [MESH:D020176] (132)  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)   Tyrosinemias [MESH:D020176] (132)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Glycogen Storage Disease Type II [MESH:D006009] (37)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease IC [MESH:C562805] (53)  Glycogen Storage Disease Type II [MESH:D006009] (37)  Glycogen Storage Disease Type I [MESH:D005953] (140)   Glycogen Storage Disease IB [MESH:C562594] (53)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Glycogen Storage Disease Type II [MESH:D006009] (37)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Dihydropyrimidine Dehydrogenase Deficiency [MESH:D054067] (88)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Hypomagnesemia 4, Renal [MESH:C567127] (225)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Tuberous Sclerosis [MESH:D014402] (635)  Exostoses, Multiple Hereditary [MESH:D005097] (154)   Stuve-Wiedemann syndrome [MESH:C537502] (66)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal [MESH:C563463] (52)  Hyperbilirubinemia, Neonatal [MESH:D051556] (469)   Jaundice, Neonatal [MESH:D007567] (290)   Jaundice, Chronic Idiopathic [MESH:D007566] (287) 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, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Keratosis [MESH:D007642] (1941)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)   Breast Neoplasms, Male [MESH:D018567] (650)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Drug Eruptions [MESH:D003875] (2697)  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)  Hair Diseases [MESH:D006201] (1891)   Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136)  Hypotrichosis [MESH:D007039] (1513)   Alopecia [MESH:D000505] (1453)  Skin Abnormalities [MESH:D012868] (1709)   Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  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)  Dyskeratosis Congenita [MESH:D019871] (185)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  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)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  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)  Skin Diseases, Vascular [MESH:D017445] (3288)   Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Iron Metabolism Disorders [MESH:D019189] (2139)  Metabolic Syndrome X [MESH:D024821] (2151)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Tyrosinemias [MESH:D020176] (132)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Glycogen Storage Disease Type II [MESH:D006009] (37)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Hypercalcemia [MESH:D006934] (1999)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  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)  Diabetes, Gestational [MESH:D016640] (1152)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Hypoglycemia [MESH:D007003] (2420)   Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hyperlipoproteinemias [MESH:D006951] (903)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipid Metabolism, Inborn Errors [MESH:D008052] (461)   Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Xanthinuria, Type I [MESH:C562584] (190)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutamine deficiency, congenital [MESH:C536832] (117)  Glutathione synthetase deficiency [MESH:C536835] (88)  Glutathionuria [MESH:C536836] (96)  Histidinemia [MESH:C538320] (87)  Hyperprolinemia [MESH:C538384] (45)  Methionine Adenosyltransferase Deficiency [MESH:C562681] (56)  Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [MESH:C562803] (33)  Glycine N-Methyltransferase Deficiency [MESH:C564683] (72)  Dimethylglycine Dehydrogenase Deficiency [MESH:C565278] (33)  Hyperhomocysteinemia [MESH:D020138] (1724)  Tyrosinemias [MESH:D020176] (132)  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)   Tyrosinemias [MESH:D020176] (132)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Glycogen Storage Disease Type II [MESH:D006009] (37)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease IC [MESH:C562805] (53)  Glycogen Storage Disease Type II [MESH:D006009] (37)  Glycogen Storage Disease Type I [MESH:D005953] (140)   Glycogen Storage Disease IB [MESH:C562594] (53)  Lactose Intolerance [MESH:D007787] (113)   Lactose Intolerance, Adult Type [MESH:C562601] (112)  Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)   Pyruvate Kinase Deficiency of Red Cells [MESH:C564858] (78)  Hyperbilirubinemia, Hereditary [MESH:D006933] (476)   Jaundice, Chronic Idiopathic [MESH:D007566] (287)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)  Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Glycogen Storage Disease Type II [MESH:D006009] (37)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Porphyrias [MESH:D011164] (917)   Porphyrias, Hepatic [MESH:D017094] (881)   Porphyria Cutanea Tarda [MESH:D017119] (766)  Purine-Pyrimidine Metabolism, Inborn Errors [MESH:D011686] (496)   Dihydropyrimidine Dehydrogenase Deficiency [MESH:D054067] (88)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Hypomagnesemia 4, Renal [MESH:C567127] (225)  Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Cortisone reductase deficiency [MESH:C536447] (136)  Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)  Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Mitochondrial Diseases [MESH:D028361] (2561)   Carnitine Palmitoyltransferase II Deficiency, Late-Onset [MESH:C563461] (52)  Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal [MESH:C563463] (52)  Mitochondrial Myopathies [MESH:D017240] (2176)  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)  Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)  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)  Hyperkalemia [MESH:D006947] (485)  Hyponatremia [MESH:D007010] (789)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Protein Deficiency [MESH:D011488] (1057)  Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Obesity, Abdominal [MESH:D056128] (115)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Adrenal Insufficiency [MESH:D000309] (1599)   Achalasia Addisonianism Alacrimia syndrome [MESH:C536008] (24)  Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Dwarfism [MESH:D004392] (698)   Laron Syndrome [MESH:D046150] (91)  Dwarfism, Pituitary [MESH:D004393] (235)   Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Pancreatic cancer, adult [MESH:C535836] (572)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gonadal Disorders [MESH:D006058] (5088)   Hypogonadism [MESH:D007006] (1123)  Disorders of Sex Development [MESH:D012734] (1637)   46, XX Disorders of Sex Development [MESH:D058489] (644)   Cortisone reductase deficiency [MESH:C536447] (136)  46, XY Disorders of Sex Development [MESH:D058490] (1060)   Androgen-Insensitivity Syndrome [MESH:D013734] (567)  Adrenogenital Syndrome [MESH:D047808] (715)   Adrenal Hyperplasia, Congenital [MESH:D000312] (674)   Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Parathyroid Diseases [MESH:D010279] (1604)   Hyperparathyroidism [MESH:D006961] (1475)   Hyperparathyroidism, Secondary [MESH:D006962] (1138)  Pituitary Diseases [MESH:D010900] (1829)   Hypopituitarism [MESH:D007018] (732)   Dwarfism, Pituitary [MESH:D004393] (235)   Short Stature, Idiopathic, Autosomal [MESH:C565805] (194)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Thyroiditis [MESH:D013966] (158)   Thyroiditis, Autoimmune [MESH:D013967] (149)   Hashimoto Disease [MESH:D050031] (98) C20. Immune System Diseases  C20. Immune System Diseases  Z. Exceptions (350)   Not Fully Specified [NFS] (350)  Immune System Diseases [MESH:D007154] (7674)   Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Juvenile [MESH:D001171] (1060)  Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Polyradiculoneuropathy [MESH:D011129] (197)   Hereditary Sensory and Autonomic Neuropathies [MESH:D009477] (172)  Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)   Glomerulopathy with fibronectin deposits [MESH:C536826] (244)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Food Hypersensitivity [MESH:D005512] (608)   Peanut Hypersensitivity [MESH:D021183] (572)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Rhinitis, Allergic, Perennial [MESH:D012221] (625)   Allergic Rhinitis [MESH:C567078] (181)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)   Angioedemas, Hereditary [MESH:D054179] (224)   Hereditary Angioedema Types I and II [MESH:D056829] (111)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Giant Lymph Node Hyperplasia [MESH:D005871] (1013)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphoma [MESH:D008223] (3684)   Hodgkin Disease [MESH:D006689] (1082)  Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)  Salmonella Infections, Animal [MESH:D012481] (604)  Cattle Diseases [MESH:D002418] (416)   Tuberculosis, Bovine [MESH:D014380] (380) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Alopecia [MESH:D000505] (1383)  Atrophy [MESH:D001284] (2603)  Plaque, Amyloid [MESH:D058225] (334)  Cysts [MESH:D003560] (133)   Megalencephalic leukoencephalopathy with subcortical cysts [MESH:C536141] (28)  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)   Emphysema [MESH:D004646] (1096)  Hyperammonemia [MESH:D022124] (322)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Tachycardia [MESH:D013610] (3339)  Chromosome Aberrations [MESH:D002869] (2352)   Micronuclei, Chromosome-Defective [MESH:D048629] (1013)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  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)   Nijmegen Breakage Syndrome-Like Disorder [MESH:C567767] (76)  Fetal Growth Retardation [MESH:D005317] (986)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Hemorrhage [MESH:D006470] (4451)   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)   Viremia [MESH:D014766] (42)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Menstruation Disturbances [MESH:D008599] (926)   Amenorrhea [MESH:D000568] (817)  Oligomenorrhea [MESH:D009839] (228)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Shock, Hemorrhagic [MESH:D012771] (2042)  Signs and Symptoms [MESH:D012816] (10659)   Chills [MESH:D023341] (644)  Edema [MESH:D004487] (3726)  Feminization [MESH:D005262] (655)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Dyskinesias [MESH:D020820] (3285)   Hyperkinesis [MESH:D006948] (1799)  Tremor [MESH:D014202] (840)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Histidinemia [MESH:C538320] (87)  Psychomotor Disorders [MESH:D011596] (576)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Seizures [MESH:D012640] (4502)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Hyperoxia [MESH:D018496] (694)  Hyperventilation [MESH:D006985] (652)  Respiratory Sounds [MESH:D012135] (713)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Virilism [MESH:D014770] (327)   Hirsutism [MESH:D006628] (323)   Cortisone reductase deficiency [MESH:C536447] (136) 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)  Silicosis [MESH:D012829] (1273) 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)  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)  Neurotoxicity Syndromes [MESH:D020258] (3323)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) 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)  Spinal Cord Injuries [MESH:D013119] (2688)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  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) D03. Heterocyclic Compounds  D03. Heterocyclic Compounds  Heterocyclic Compounds [MESH:D006571] (56330)   Heterocyclic Compounds, 1-Ring [MESH:D006573] (30631)   Dioxoles [MESH:D004149] (442)   Benzodioxoles [MESH:D052117] (148)   Piperonyl Butoxide [MESH:D010882] (9)  Heterocyclic Compounds, 2-Ring [MESH:D006574] (24204)   Benzodioxoles [MESH:D052117] (148)   Piperonyl Butoxide [MESH:D010882] (9) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Histidinemia [MESH:C538320] (87)  Psychomotor Disorders [MESH:D011596] (250)   Phosphoglycerate Dehydrogenase Deficiency [MESH:C566618] (83)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Hoyeraal Hreidarsson syndrome [MESH:C536068] (154)  Histidinemia [MESH:C538320] (87)  Sexual and Gender Disorders [MESH:D019968] (624)   Disorders of Sex Development [MESH:D012734] (609)   46, XX Disorders of Sex Development [MESH:D058489] (375)   Cortisone reductase deficiency [MESH:C536447] (136)