oculocutaneous albinism type 4 Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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Genes

1 genes associated with the disease oculocutaneous albinism type 4 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
SLC45A2 solute carrier family 45, member 2