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Disease Ontology Browser
cone-rod dystrophy 15 (DOID:0111021)
Alliance: disease page
Synonyms: CORD15
Alt IDs: OMIM:613660
Definition: A cone-rod dystrophy that has_material_basis_in homozygous mutation in the CDHR1 gene on chromosome 10q23.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory