Fatal liver failure in infancy

Symptom Information:

Symptom ID: HPO:0006583
Synonyms:
Fatal liver failure in infancy (occasional) [OMIM:Fatal liver failure in infancy (occasional)]
Quality:
Cross references:
OMIM: "Fatal liver failure in infancy (occasional)" [OMIM:Fatal liver failure in infancy (occasional)]
Is a (Direct Parents):
HPO         Hepatic failure
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)
                      Fatal liver failure in infancy(HPO:0006583)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

MEGDEL syndrome (Orphanet:352328)
NIEMANN-PICK DISEASE, TYPE C1 (OMIM:257220)
Neonatal hemochromatosis (Orphanet:446)