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cone-rod dystrophy 2 | RareConnect | RareConnect.io

/cone-rod dystrophy

/retinitis pigmentosa

/CRX-related retinopathy

/cone-rod dystrophy 2

cone-rod dystrophy 2

Rare Disease

MONDO:0007362

Also Known As

CORD2CRD2CRX cone-rod dystrophyRCRD2cone-rod dystrophy 2cone-rod dystrophy caused by mutation in CRXcone-rod dystrophy type 2cone-rod retinal dystrophy 2cone-rod retinal dystrophy-2retinal cone-rod dystrophy 2cone-rod dystrophycone-rod retinal dystrophyretinal cone-rod dystrophy

Definition

Any cone-rod dystrophy in which the cause of the disease is a mutation in the CRX gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:120970 ↗

GARD

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dominant pericentral pigmentary retinopathy

MONDO:0008381

late-adult onset retinitis pigmentosa

MONDO:0009984

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