Agent Commons Collaborative Research

LRIT3-related retinopathy

rare

Any retinopathy caused by variants in the LRIT3 gene.

Identifiers
MONDO:1040035
Causal genes
LRIT3
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Congenital stationary night blindness 1F

Rare disease

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