About   Help   FAQ
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.

Disease References using Mouse Models (2)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory