Elevated hepatic transaminases
Symptom Information:
Symptom ID: | HPO:0002910 | |||||||||||||||||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the liver(HPO:0001392) Elevated hepatic transaminases(HPO:0002910) MedDRA: Investigations(MedDRA:10022891) Hepatobiliary investigations(MedDRA:10019809) Liver function analyses(MedDRA:10024689) Elevated hepatic transaminases(HPO:0002910) |
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Database Frequency: | 158 / 7739 | |||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
AICARDI-GOUTIERES SYNDROME 3 | (OMIM:610329) |
AICARDI-GOUTIERES SYNDROME 4 | (OMIM:610333) |
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
Acute infantile liver failure-multisystemic involvement syndrome | (Orphanet:370088) |
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Adult Still's disease | (Orphanet:829) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Alpers syndrome | (Orphanet:726) |
Alpha-1-antitrypsin deficiency | (Orphanet:60) |
Alström syndrome | (Orphanet:64) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Ataxia-telangiectasia | (Orphanet:100) |
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4 | (OMIM:214950) |
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5 | (OMIM:616278) |
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 4 | (OMIM:615982) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Beta-thalassemia major | (Orphanet:231214) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Biliary atresia | (Orphanet:30391) |
Budd-Chiari syndrome | (Orphanet:131) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
COG4-CDG | (Orphanet:263501) |
CONGENITAL DISORDER OF DEGLYCOSYLATION | (OMIM:615273) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Carnitine palmitoyl transferase II deficiency | (Orphanet:157) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Carnitine uptake deficiency | (Orphanet:158) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Cholestasis - lymphedema | (Orphanet:1414) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Choreoacanthocytosis | (Orphanet:2388) |
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome | (Orphanet:309854) |
Citrullinemia type II | (Orphanet:247585) |
Classical homocystinuria | (Orphanet:394) |
Combined oxidative phosphorylation defect type 2 | (Orphanet:254920) |
Combined oxidative phosphorylation defect type 9 | (Orphanet:319509) |
Common variable immunodeficiency | (Orphanet:1572) |
Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
Congenital bile acid synthesis defect type 2 | (Orphanet:79303) |
Congenital bile acid synthesis defect type 3 | (Orphanet:79302) |
Congenital bile acid synthesis defect type 4 | (Orphanet:79095) |
Congenital disorder of glycosylation | (Orphanet:137) |
Congenital intrauterine infection-like syndrome | (Orphanet:1229) |
Congenital toxoplasmosis | (Orphanet:858) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
DK1-CDG | (Orphanet:91131) |
DPAGT1-CDG | (Orphanet:86309) |
DPM1-CDG | (Orphanet:79322) |
DPM3-CDG | (Orphanet:263494) |
Disorder of bile acid synthesis | (Orphanet:79168) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Early-onset familial noncirrhotic portal hypertension | (ORPHA:494348) |
Fetal Gaucher disease | (Orphanet:85212) |
GLYCOGEN STORAGE DISEASE IXc | (OMIM:613027) |
Gaucher disease type 2 | (Orphanet:77260) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
Glycogen storage disease due to hepatic glycogen synthase deficiency | (Orphanet:2089) |
Glycogen storage disease due to liver phosphorylase kinase deficiency | (Orphanet:264580) |
HERNS syndrome | (Orphanet:63261) |
Hairy cell leukemia variant | (Orphanet:300878) |
Hashimoto-Pritzker syndrome | (Orphanet:99872) |
Hemochromatosis type 3 | (Orphanet:225123) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemochromatosis, type 2B | (OMIM:613313) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hereditary fructose intolerance | (Orphanet:469) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Hurler syndrome | (Orphanet:93473) |
Hypermethioninemia due to glycine N-methyltransferase deficiency | (Orphanet:289891) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
INFANTILE LIVER FAILURE SYNDROME 2 | (OMIM:615486) |
INTERSTITIAL NEPHRITIS, KARYOMEGALIC | (OMIM:614817) |
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | (Orphanet:352563) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Infantile regressive hypertriglyceridemia and hepatosteatosis | (Orphanet:300293) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Joubert syndrome 1 | (OMIM:213300) |
Joubert syndrome 2 | (OMIM:608091) |
Joubert syndrome 21 | (OMIM:615636) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
LIPOYLTRANSFERASE 1 DEFICIENCY | (OMIM:616299) |
Lathosterolosis | (Orphanet:46059) |
Leigh syndrome | (Orphanet:506) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Low phospholipid associated cholelithiasis | (Orphanet:69663) |
Lyell syndrome | (Orphanet:537) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 | (OMIM:615453) |
Mandibular hypoplasia-deafness-progeroid syndrome | (Orphanet:363649) |
Marburg hemorrhagic fever | (Orphanet:99826) |
McCune-Albright syndrome | (Orphanet:562) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Medium chain acyl-CoA dehydrogenase deficiency | (Orphanet:42) |
Mevalonic aciduria | (Orphanet:29) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | (Orphanet:369897) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE | (OMIM:602114) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Navajo neurohepatopathy | (Orphanet:255229) |
Nephronophthisis 3 | (OMIM:604387) |
Neutral lipid storage myopathy | (Orphanet:98908) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER) | (OMIM:614883) |
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) | (OMIM:614886) |
PGM1-CDG | (Orphanet:319646) |
PMM2-CDG | (Orphanet:79318) |
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY | (OMIM:615895) |
PREECLAMPSIA/ECLAMPSIA 1 | (OMIM:189800) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 | (OMIM:610131) |
PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED | (OMIM:300752) |
Pearson syndrome | (Orphanet:699) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polyglucosan body myopathy type 1 | (ORPHA:397937) |
Preeclampsia | (Orphanet:275555) |
Primary sclerosing cholangitis | (Orphanet:171) |
Progressive familial intrahepatic cholestasis type 3 | (Orphanet:79305) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Reynolds syndrome | (Orphanet:779) |
SRD5A3-CDG | (Orphanet:324737) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Stevens-Johnson syndrome | (Orphanet:36426) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5 | (OMIM:615506) |
TMEM165-CDG | (Orphanet:314667) |
TRAPS syndrome | (Orphanet:32960) |
Tyrosinemia type 1 | (Orphanet:882) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
XFE PROGEROID SYNDROME | (OMIM:610965) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |