Oculocutaneous albinism type 4 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Oculocutaneous albinism type 4 (OCA4) is a type of OCA (see this term) characterized by varying degrees of skin and hair hypopigmentation, numerous ocular changes and misrouting of the optic nerves at the chiasm. (Orphanet Rare Disease Ontology, Orphanet_79435)
External Link http://www.omim.org/entry/606574
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Genes

1 genes associated with the Oculocutaneous albinism type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SLC45A2 solute carrier family 45, member 2