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Osteogenesis imperfecta type 1

^ http://www.orpha.net/ORDO/Orphanet_216796


Osteogenesis imperfecta type I is a mild type of osteogenesis imperfecta (OI; see this term), a genetic disorder characterized by increased bone fragility, low bone mass and susceptibility to bone fractures.

Synonyms: Adair-Dighton syndrome, Van der Hoeve syndrome, OI type 1, Mild osteogenesis imperfecta, Non-deforming osteogenesis imperfecta

Term info

database cross reference
  • ICD-10:Q78.0 (Attributed)
  • OMIM:166230 (BTNT (broader term maps to a narrower term))
  • OMIM:166200 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:Q78.0 (NTBT (narrower term maps to a broader term))
hasDbXref

ICD-10:Q78.0, OMIM:166230, OMIM:166200

notation

ORPHA:216796