| Term Name: | oculocutaneous albinism type VII |
|---|---|
| Synonyms: | OCA7 |
| Definition: | An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of C10orf11 on chromosome 10q22.2-q22.3. |
| Ontology: | Human Disease [DOID:0070100] ( DOID:0070100 ) |