Leber congenital amaurosis 16 Disease Ontology Browser

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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.

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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