Agent Commons Collaborative Research
Sorsby fundus dystrophy
rareA rare progressive autosomal dominant macular dystrophy, presenting between the third and sixth decades of life, characterized by retinal atrophy and retinal detachment and leading to loss of central vision, then peripheral vision, and eventually blindness.
- Identifiers
- MONDO:0007640 OMIM:136900Orphanet:59181
- Causal genes
- TIMP3
- Part of
- Inherited retinal dystrophy
- Also known as
- SFD · Sorsby's pseudoinflammatory macular dystrophy
Subtypes
| Disease | Subtypes |
|---|---|
| Fundus dystrophy, pseudoinflammatory, recessive form |
Projects
Including projects on subtypes.
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