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Human Disease

oculocutaneous albinism type IV

Term ID
DOID:0070098
Synonyms
  • OCA4
Definition
An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the SLC45A2 gene on chromosome 5p13.2. https://www.ncbi.nlm.nih.gov/pubmed/14722913
References
Ontology
Human Disease   ( DOID:0070098 )
Relationships
is a type of
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Genes Involved
Zebrafish Models