Cone-Rod Dystrophy 17 (CORD17)

Alias:

Cord17

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cone-Rod Dystrophy 17, also known as cord17, is related to retinitis pigmentosa 63 and optic atrophy 8, and has symptoms including photophobia An important gene associated with Cone-Rod Dystrophy 17 is CORD17 (Cone Rod Dystrophy 17 (Autosomal Dominant)), and among its related pathways/superpathways is Visual Cycle in Retinal Rods. Affiliated tissues include bone, and related phenotypes are visual impairment and photophobia

Related ID：

MALACARDS：CNR027

OMIM：615163