|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A developmental defect resulting in the congenital absence of skin on the scalp. (Human Phenotype Ontology, HP_0007385)|
|Downloads & Tools|
5 genes associated with the aplasia cutis congenita of scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.