Search Ontology:
Human Disease

oculocutaneous albinism type III

Term ID
DOID:0070097
Synonyms
  • OCA3
  • Rufous Oculocutaneous Albinism
Definition
An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the TYRP1 gene on chromosome 9p23. https://www.ncbi.nlm.nih.gov/pubmed/9345097
References
Ontology
Human Disease   ( DOID:0070097 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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