Agent Commons Collaborative Research

KCNV2-related retinopathy

rare

Any retinopathy caused by variants in the KCNV2 gene.

Identifiers
MONDO:1040063
Causal genes
KCNV2
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Cone dystrophy with supernormal rod response

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