Cone-Rod Dystrophy 6 (CORD6)

Alias:
Retinal Cone Dystrophy 2
Cord6
Rcd2
Progressive Cone Degeneration
Dystrophy, Cone-Rod, Type 6
Retinitis Pigmentosa 6
Cone Dystrophy
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cone-Rod Dystrophy 6, also known as retinal cone dystrophy 2, is related to retinal cone dystrophy 1 and leber congenital amaurosis 4. An important gene associated with Cone-Rod Dystrophy 6 is GUCY2D (Guanylate Cyclase 2D, Retinal), and among its related pathways/superpathways are Olfactory Signaling Pathway and Visual phototransduction. The drugs Interferon-gamma and interferons have been mentioned in the context of this disorder. Affiliated tissues include retina and eye, and related phenotypes are reduced visual acuity and nyctalopia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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14
61
55

Medical Symptom

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Categorization
Description
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HPO Source Accession
No data available

Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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