Acute hepatic failure

Symptom Information:

Symptom ID: HPO:0006554
Synonyms:
Acute liver failure [HPO:0006554]
Acute hepatic failure (disorder) [Orphanet:29300]
Liver Failure, Acute [Orphanet:29300]
Acute hepatic failure [OMIM:Acute hepatic failure]
Acute liver failure [OMIM:Acute liver failure]
Acute hepatic failure [Orphanet:29300]
Acute hepatic failure [MedDRA:10000804]
Fulminant hepatic failure [MedDRA:10000804]
Acute liver failure [MedDRA:10000804]
Acute on chronic hepatic failure [MedDRA:10000804]
Fulminant hepatic failure (in 2 sibs) [OMIM:Fulminant hepatic failure (in 2 sibs)]
Fulminant hepatic failure (reported in 1 patient) [OMIM:Fulminant hepatic failure (reported in 1 patient)]
Quality:
Cross references:
Orphanet:29300 "Acute hepatic failure" [Orphanet:29300]
OMIM: "Acute hepatic failure" [OMIM:Acute hepatic failure]
OMIM: "Acute liver failure" [OMIM:Acute liver failure]
OMIM: "Fulminant hepatic failure (in 2 sibs)" [OMIM:Fulminant hepatic failure (in 2 sibs)]
OMIM: "Fulminant hepatic failure (reported in 1 patient)" [OMIM:Fulminant hepatic failure (reported in 1 patient)]
UMLS:C0162557 "Liver Failure, Acute" [Orphanet:29300]
Is a (Direct Parents):
Orphanet Hepatic failure
HPO         Hepatic failure
MedDRA Hepatic failure and associated disorders
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)
                Decreased liver function(HPO:0001410)
                   Hepatic failure(HPO:0001399)
                      Acute hepatic failure(HPO:0006554)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
    Hepatic and hepatobiliary disorders(MedDRA:10019654)
       Hepatic failure and associated disorders(MedDRA:10019664)
          Acute hepatic failure(HPO:0006554)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (OMIM:231530)
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins (Orphanet:217371)
Acute infantile liver failure-multisystemic involvement syndrome (Orphanet:370088)
Budd-Chiari syndrome (Orphanet:131)
Choreoacanthocytosis (Orphanet:2388)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Ebola hemorrhagic fever (Orphanet:319218)
Familial Mediterranean fever (Orphanet:342)
Focal dermal hypoplasia (Orphanet:2092)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hydatidosis (Orphanet:400)
Lyell syndrome (Orphanet:537)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 (OMIM:615453)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Navajo neurohepatopathy (Orphanet:255229)
Neonatal hemochromatosis (Orphanet:446)
Stevens-Johnson syndrome (Orphanet:36426)
Tyrosinemia type 1 (Orphanet:882)
Wolcott-Rallison syndrome (Orphanet:1667)
Yellow fever (Orphanet:99829)