|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Microcephaly (HP:0000252) that is present already at the time of birth. (Human Phenotype Ontology, HP_0011451)|
|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.