GUCY2D retinopathy
MONDO:0100454Mondo
Findings
No curated finding names GUCY2D retinopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any inherited retinal dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.
Definition from the Mondo Disease Ontology (MONDO:0100454), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
1 name
Resolves to: GUCY2D retinopathy
- Also called
- retinopathy caused by mutation in GUCY2D