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Disease Ontology Browser
Leber congenital amaurosis 15 (DOID:0110189)
Alliance: disease page
Synonyms: LCA15
Alt IDs: OMIM:613843, ICD10CM:H35.5
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the TULP1 gene on chromosome 6p21.3.


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
01/24/2023
MGI 6.22
The Jackson Laboratory