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Disease Ontology Browser
cone-rod dystrophy 2 (DOID:0111005)
Alliance: disease page
Synonyms: cone-rod retinal dystrophy 2; CORD2; CRD2; RCRD2; retinal cone-rod dystrophy 2
Alt IDs: OMIM:120970
Definition: A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13.


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
03/03/2020
MGI 6.15
The Jackson Laboratory