infantile encephalopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Encephalopathy with onset in the infantile period. (Human Phenotype Ontology, HP_0007105)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007105
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Genes

4 genes associated with the infantile encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
D2HGDH D-2-hydroxyglutarate dehydrogenase
GCDH glutaryl-CoA dehydrogenase
STXBP1 syntaxin binding protein 1
TSEN54 TSEN54 tRNA splicing endonuclease subunit