oculocutaneous albinism type VI

Term ID

DOID:0080614

Synonyms

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

References

• OMIM:113750

Ontology

Human Disease   ( DOID:0080614 )