Microvesicular hepatic steatosis
Symptom Information:
Symptom ID: | HPO:0001414 | |||
Synonyms: |
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Cross references: |
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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) Microvesicular hepatic steatosis(HPO:0001414) MedDRA: |
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Database Frequency: | 9 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Alpers syndrome | (Orphanet:726) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Dilated cardiomyopathy with ataxia | (Orphanet:66634) |
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | (Orphanet:352563) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Navajo neurohepatopathy | (Orphanet:255229) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |