Oculocutaneous albinism type 7 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Oculocutaneous albinism type 7 (OCA7), formerly called OCA5, is a form of oculocutaneous albinism (OCA; see this term) characterized by skin and hair hypopigmentation, nystagmus and iris transillumination. (Orphanet Rare Disease Ontology, Orphanet_352745)
External Link http://www.omim.org/entry/615179
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Genes

1 genes associated with the Oculocutaneous albinism type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
C10ORF11 chromosome 10 open reading frame 11