Macrovesicular hepatic steatosis
Symptom Information:
Symptom ID: | HPO:0001403 | |||
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) Hepatic steatosis(HPO:0001397) Macrovesicular hepatic steatosis(HPO:0001403) MedDRA: |
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Database Frequency: | 7 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Navajo neurohepatopathy | (Orphanet:255229) |