Macrovesicular hepatic steatosis

Symptom Information:

Symptom ID: HPO:0001403
Synonyms:
Macrovesicular steatosis [HPO:0001403]
Macrovesicular steatosis [OMIM:Macrovesicular steatosis]
Macrovesicular steatosis (1 patient) [OMIM:Macrovesicular steatosis (1 patient)]
Quality:
Cross references:
OMIM: "Macrovesicular steatosis" [OMIM:Macrovesicular steatosis]
OMIM: "Macrovesicular steatosis (1 patient)" [OMIM:Macrovesicular steatosis (1 patient)]
Is a (Direct Parents):
HPO         Hepatic steatosis
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:
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)