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Metadata
ID DOID:0080614
Name oculocutaneous albinism type VI
Definition An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of the SLC24A5 gene on chromosome 15q21.1.
https://www.omim.org/entry/203100?search=albinism%20type%20ia&highlight=albinism%20ia%20type
Xrefs

OMIM:113750

Parent Relationships

is_a oculocutaneous albinism

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