Search Ontology:
Human Disease
oculocutaneous albinism type III
- Term ID
- DOID:0070097
- Synonyms
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- OCA3
- Rufous Oculocutaneous Albinism
- Definition
- An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the TYRP1 gene on chromosome 9p23. https://www.ncbi.nlm.nih.gov/pubmed/9345097
- References
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- GARD:4039
- MIM:203290
- Ontology
- Human Disease ( DOID:0070097 )
- is a type of
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Genes Involved
Zebrafish Models