OBO ID: DOID:0080614
Term Name: oculocutaneous albinism type VI Search Ontology:
Synonyms:
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
References:
Ontology: Human Disease   ( DOID:0080614 )
OTHER oculocutaneous albinism type VI PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC24A5 Albinism, oculocutaneous, type VI 113750
[Skin/hair/eye pigmentation 4, fair/dark skin] 113750
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None