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Disease Ontology Browser
Leber congenital amaurosis 7 (DOID:0110333)
Alliance: disease page
Synonyms: LCA7
Alt IDs: OMIM:613829, ICD10CM:H35.5
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.

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 6.15
The Jackson Laboratory