oculocutaneous albinism type V

Term ID

DOID:0070099

Synonyms

• OCA5

Definition

An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the OCA5 gene on chromosome 4q24. https://www.ncbi.nlm.nih.gov/pubmed/23050561

References

• OMIM:615312

Ontology

Human Disease   ( DOID:0070099 )