|OBO ID: DOID:0110079|
|Term Name:||Leber congenital amaurosis 8||Search Ontology:|
|Definition:||A Leber congenital amaurosis that is characterized by night blindness and thick unlaminated retinas and has_material_basis_in mutation in the CRB1 gene on chromosome 1q31-q32. https://www.ncbi.nlm.nih.gov/pubmed/11231775|
|Ontology:||Human Disease (DOID:0110079)|
|is a type of:||
OTHER Leber congenital amaurosis 8 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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