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Disease Ontology Browser
Leber congenital amaurosis 11 (DOID:0110216)
Alliance: disease page
Synonyms: LCA11
Alt IDs: OMIM:613837, ICD10CM:H35.5
Definition: A Leber congenital amaurosis that has_material_basis_in mutation n the IMPDH1 gene on chromosome 7q31.3-q32.


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
09/05/2019
MGI 6.14
The Jackson Laboratory