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Disease Ontology Browser
Leber congenital amaurosis 8 (DOID:0110079)
Alliance: disease page
Synonyms: LCA8
Alt IDs: OMIM:613835, ICD10CM:H35.5
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.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory