Fulminant hepatic failure
Symptom Information:
Symptom ID: | HPO:0004448 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) Fulminant hepatic failure(HPO:0004448) MedDRA: |
||
Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY | (OMIM:231530) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency | (Orphanet:71212) |
Wilson disease | (Orphanet:905) |