98041000119107: Family history of osteogenesis imperfecta (situation)

• SNOMED CT Concept\Situation with explicit context (situation)\...
• \Finding with explicit context (situation)\Family history of clinical finding\Family history of disorder\...
• \Family history of development disorder\Family history of congenital malformation\FH: Cong. orthopedic anomaly\Family history of osteogenesis imperfecta
• \FH: Musculoskeletal disease\FH: Cong. orthopedic anomaly\Family history of osteogenesis imperfecta
• \Family history of congenital disease (situation)\Family history of congenital malformation\FH: Cong. orthopedic anomaly\Family history of osteogenesis imperfecta
• \Family history with explicit context (situation)\Family history of clinical finding\Family history of disorder\...
• \Family history of development disorder\Family history of congenital malformation\FH: Cong. orthopedic anomaly\Family history of osteogenesis imperfecta
• \FH: Musculoskeletal disease\FH: Cong. orthopedic anomaly\Family history of osteogenesis imperfecta
• \Family history of congenital disease (situation)\Family history of congenital malformation\FH: Cong. orthopedic anomaly\Family history of osteogenesis imperfecta

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3042644015	Family history of osteogenesis imperfecta	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3042666010	Family history of osteogenesis imperfecta (situation)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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