Human Phenotype Ontology 
Grandparent Node:
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Lipid accumulation in hepatocytes (HP:0006561)help
Parent Node:
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Hepatic steatosis (HP:0001397)help
..Starting node
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Acute hepatic steatosis (HP:0006573)help
Term ID: 6573
Name: Acute hepatic steatosis
Synonym: Acute fatty liver
Definition: An acute form of hepatic steatosis.
Comments:
Reference: HP:0006573
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDiffuse hepatic steatosis (HP:0006555) help
..expandMacrovesicular hepatic steatosis (HP:0001403) help
..expandMicrovesicular hepatic steatosis (HP:0001414) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006573HP:0006573Acute hepatic steatosis0CYP7A1 CL E G H1581209902ORPHA11452651118455
HP:0006573HP:0006573Acute hepatic steatosis0MCCC1 CL E G H569222102003 Methylcrotonyl-CoA carboxylase 1 deficiency210200CN028786OMIM17206936609010
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :CYP7A1 MCCC1

Diseases (2) :209902 210200
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.