microvesicular hepatic steatosis Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A form of hepatic steatosis characterized by the presence of small, lipid-laden vesicles in the affected hepatocytes. (Human Phenotype Ontology, HP_0001414)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0001414
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Genes

8 genes associated with the microvesicular hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ACAD9	acyl-CoA dehydrogenase family, member 9
BCS1L	BC1 (ubiquinol-cytochrome c reductase) synthesis-like
DNAJC19	DnaJ (Hsp40) homolog, subfamily C, member 19
LRPPRC	leucine-rich pentatricopeptide repeat containing
MPV17	MpV17 mitochondrial inner membrane protein
MRPL44	mitochondrial ribosomal protein L44
POLG	polymerase (DNA directed), gamma
TRMU	tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase