Acute hepatic failure
Symptom Information:
Symptom ID: | HPO:0006554 | ||||||||||||
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) 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) |
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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) |