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- B80fb87682aa4f6ca88f32a46e4a1581f hasDbXref "Orphanet:337" @default.
- B80fb87682aa4f6ca88f32a46e4a1581f type Axiom @default.
- B80fb87682aa4f6ca88f32a46e4a1581f annotatedProperty IAO_0000115 @default.
- B80fb87682aa4f6ca88f32a46e4a1581f annotatedSource MONDO_0007606 @default.
- B80fb87682aa4f6ca88f32a46e4a1581f annotatedTarget "Fibrodysplasia 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." @default.