congenital microcephaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Microcephaly (HP:0000252) that is present already at the time of birth. (Human Phenotype Ontology, HP_0011451)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011451
Similar Terms
Downloads & Tools

Genes

2 genes associated with the congenital microcephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PHGDH phosphoglycerate dehydrogenase
RBBP8 retinoblastoma binding protein 8