aphakia, congenital primary Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_11367)
External Link http://www.omim.org/entry/610256
Similar Terms
Downloads & Tools


1 genes associated with the aphakia, congenital primary phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FOXE3 forkhead box E3