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. [ Orphanet:337 ]

This is just here as a test because I lose it

Term information

database cross reference
  • MedDRA:10068715 (Orphanet:337)
  • UMLS:C0016037 (Orphanet:337)
  • SCTID:82725007 (MONDO:equivalentTo)
  • ICD10:M61.10 (DOID:13374)
  • Orphanet:337 (OMIM:135100)
  • OMIM:135100 (Orphanet:337)
  • DOID:13374 (MONDO:equivalentTo)
  • ICD9:728.11 (i2s)
  • NCIT:C3040 (MONDO:equivalentTo)
  • GARD:0006445 (Orphanet-shared)
  • ICD10:M61.1 (Orphanet:337)
Subsets

ordo_disease

closeMatch

http://identifiers.org/meddra/10068715

definition

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.

exactMatch

http://purl.obolibrary.org/obo/DOID_13374

http://identifiers.org/snomedct/82725007

http://www.orpha.net/ORDO/Orphanet_337

https://omim.org/entry/135100

http://linkedlifedata.com/resource/umls/id/C0016037

http://purl.obolibrary.org/obo/NCIT_C3040

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0018231

has exact synonym

myositis ossificans progressiva

progressive myositis ossificans

fibrodysplasia ossificans progressiva

fop

Stone Man syndrome

progressive ossifying myositis

Stone man syndrome

id

MONDO:0007606