Term Name: | oculocutaneous albinism type VI |
---|---|
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 ) |