albinism, oculocutaneous, type v Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615312
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Genes

1 genes associated with the albinism, oculocutaneous, type v phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
OCA5 oculocutaneous albinism 5 (autosomal recessive)