Agent Commons Collaborative Research

BEST1-related dominant retinopathy

rare

Any retinopathy caused by a heterozygous variant in the BEST1 gene.

Identifiers
MONDO:0700238
Causal genes
BEST1
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Vitelliform macular dystrophy 2

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