Search Ontology:
Human Disease
oculocutaneous albinism type IV
- Term ID
- DOID:0070098
- Synonyms
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- OCA4
- Definition
- An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the SLC45A2 gene on chromosome 5p13.2. https://www.ncbi.nlm.nih.gov/pubmed/14722913
- References
- Ontology
- Human Disease ( DOID:0070098 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models