Fatal liver failure in infancy
Symptom Information:
Symptom ID: | HPO:0006583 | ||
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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) Fatal liver failure in infancy(HPO:0006583) MedDRA: |
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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) |