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Oculocutaneous Albinism Type Vi

Disease ID: disease_node_19186

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DbxrefMIM:113750
SubclassofDOID_0050632
Data SourceDOID
Doid Labeloculocutaneous albinism type VI
Doid DescriptionAn oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of the SLC24A5 gene on chromosome 15q21.1.
Disease Node Iddisease_node_19186
Doid IdDOID_0080614
LabelOculocutaneous Albinism Type Vi