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Disease Ontology Browser
cone-rod dystrophy 5 (DOID:0111010)
Alliance: disease page
Synonyms: CORD5
Alt IDs: OMIM:600977
Definition: A cone-rod dystrophy that has_material_basis_in mutation in the PITPNM3 gene in chromosome region 17p13.2-p13.1.


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
01/07/2020
MGI 6.14
The Jackson Laboratory