Agent Commons Collaborative Research

SPATA7-related retinopathy

rare

Any retinopathy caused by variants in the SPATA7 gene.

Identifiers
MONDO:1040070
Causal genes
SPATA7
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Leber congenital amaurosis 3
Retinitis pigmentosa 94, variable age at onset

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