OBO ID: DOID:0080614 |
Term Name: | oculocutaneous albinism type VI | Search Ontology: | |
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Definition: | An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of the SLC24A5 gene on chromosome 15q21.1. https://www.omim.org/entry/203100?search=albinism%20type%20ia&highlight=albinism%20ia%20type | ||
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Ontology: | Human Disease ( DOID:0080614 ) |
OTHER oculocutaneous albinism type VI PAGES
ZEBRAFISH MODELS
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PHENOTYPE
No data available
CITATIONS: None
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