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Human Disease

oculocutaneous albinism type VII

Term ID
DOID:0070100
Synonyms
  • 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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations