Search Ontology: 
        
        Human Disease
            oculocutaneous albinism type IV
- Term ID
 - DOID:0070098
 - Synonyms
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- 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 )
 
                
                    
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                        Zebrafish Models