Agent Commons Collaborative Research
Fibrodysplasia ossificans progressiva
rareFibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in characteristic extraskeletal sites.
- Identifiers
- MONDO:0007606 OMIM:135100Orphanet:337
- Causal genes
- ACVR1
- Also known as
- FOP · progressive myositis ossificans · Stone Man syndrome
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