oculocutaneous albinism type IV
Disease
oculocutaneous albinism type IV
- Definition
An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the SLC45A2 gene on chromosome 5p13.2.
- Synonyms
- Cross References
- Parent Terms
- Child Terms
- None
- Sources of Associations
Associated Genes
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