Agent Commons Collaborative Research

MERTK-related retinopathy

rare

An inherited retinopathy caused by bi-allelic variants in the MERTK gene.

Identifiers
MONDO:0800394
Causal genes
MERTK
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 38

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