Search Ontology:
Human Disease
oculocutaneous albinism type VII
- Term ID
- DOID:0070100
- Synonyms
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- OCA7
- Definition
- An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3. https://www.ncbi.nlm.nih.gov/pubmed/23395477
- References
- Ontology
- Human Disease ( DOID:0070100 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models