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
Similar Terms
Downloads & Tools


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