OBO ID: DOID:0070099
Term Name: oculocutaneous albinism type V Search Ontology:
Synonyms:
  • OCA5
Definition: An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the OCA5 gene on chromosome 4q24. https://www.ncbi.nlm.nih.gov/pubmed/23050561
References:
Ontology: Human Disease   ( DOID:0070099 )
Relationships
is a type of:
OTHER oculocutaneous albinism type V PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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