|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A developmental defect resulting in the congenital absence of skin on the scalp in the parietal area. (Human Phenotype Ontology, HP_0004476)|
|Downloads & Tools|
1 genes associated with the aplasia cutis congenita over parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|ARHGAP31||Rho GTPase activating protein 31|