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Disease Ontology Browser
Leber congenital amaurosis 12 (DOID:0110080)
Synonyms: LCA12
Alt IDs: OMIM:610612, ICD10CM:H35.5, ORDO:65
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.08
The Jackson Laboratory