Cone-Rod Dystrophy 1 (CORD1)

Alias:

Cord1

Crd1

Cone-Rod Retinal Dystrophy-1

Retinitis Pigmentosa 1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cone-Rod Dystrophy 1, also known as cord1, is related to cone-rod dystrophy, x-linked, 1 and cone-rod dystrophy 9. An important gene associated with Cone-Rod Dystrophy 1 is CORD1 (Cone Rod Dystrophy 1 (Autosomal Dominant)), and among its related pathways/superpathways are Phosphodiesterases in neuronal function and Visual signal transduction: Cones. Affiliated tissues include skin, and related phenotypes are intellectual disability and hearing impairment

Related ID：

MALACARDS：CNR003

OMIM：600624

MESH：C563469