| Term Name: | oculocutaneous albinism type VI |
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| Synonyms: | |
| Definition: | An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of the SLC24A5 gene on chromosome 15q21.1. |
| Ontology: | Human Disease [DOID:0080614] ( DOID:0080614 ) |