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Disease Ontology Browser
Leber congenital amaurosis 9 (DOID:0110005)
Alliance: disease page
Synonyms: LCA9
Alt IDs: OMIM:608553, ICD10CM:H35.5
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36.

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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MGI 6.11
The Jackson Laboratory