Search Ontology:
Human Disease

oculocutaneous albinism type V

Term ID
DOID:0070099
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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