Cone-Rod Dystrophy 11 (CORD11)

Alias:
Cord11
Dystrophy, Cone-Rod, Type 11
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cone-Rod Dystrophy 11, also known as cord11, is related to occult macular dystrophy and stargardt disease 1. An important gene associated with Cone-Rod Dystrophy 11 is RAX2 (Retina And Anterior Neural Fold Homeobox 2), and among its related pathways/superpathways is Bardet-Biedl syndrome. Affiliated tissues include retina and eye, and related phenotypes are photophobia and pallor
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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6
31
2

Medical Symptom

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Description
HPO Frequency
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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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