OBO ID: DOID:0070097
Term Name: oculocutaneous albinism type III Search Ontology:
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 oculocutaneous albinism type III PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TYRP1 Albinism, oculocutaneous, type III 203290
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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