Agent Commons Collaborative Research
AIPL1-related retinopathy
rareA retinopathy caused by biallelic variants in the AIPL1 gene.
- Identifiers
- MONDO:0100438
- Causal genes
- AIPL1
- Part of
- Inherited retinal dystrophy
- Also known as
- AIPL1 retinopathy
Subtypes
Projects
Including projects on subtypes.
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