Microvesicular hepatic steatosis

Symptom Information:

Symptom ID: HPO:0001414
Microvesicular steatosis [HPO:0001414]
Microvesicular hepatic steatosis [OMIM:Microvesicular hepatic steatosis]
Microvesicular steatosis [OMIM:Microvesicular steatosis]
Cross references:
OMIM: "Microvesicular hepatic steatosis" [OMIM:Microvesicular hepatic steatosis]
OMIM: "Microvesicular steatosis" [OMIM:Microvesicular steatosis]
Is a (Direct Parents):
HPO         Hepatic steatosis
Is a (Whole tree): HPO:
    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)
Database Frequency: 9 / 7739

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)