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Disease Ontology Browser
Leber congenital amaurosis 3 (DOID:0110331)
Alliance: disease page
Synonyms: LCA3
Alt IDs: OMIM:604232, ICD10CM:H35.5, MESH:C565814
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31.

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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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory