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Disease Ontology Browser
Leber congenital amaurosis 16 (DOID:0110118)
Alliance: disease page
Synonyms: LCA16
Alt IDs: OMIM:614186, ICD10CM:H35.5
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the KCNJ13 gene on chromosome 2q37.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory