inherited retinal dystrophy
MONDO:0019118Also known as: fundus dystrophy, familial retinal dystrophy, genetic retinal dystrophy, hereditary retinal degeneration, hereditary retinal dystrophy
- MONDO:
- MONDO:0019118
- Orphanet:
- 71862 ↗
Rare disease41 associated genes
Description
An instance of retinal degeneration that is caused by an inherited modification of the individual's genome.
Associated genes
+31 more genes — install the extension to see the full list inline on any page.