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254110009: Osteogenesis imperfecta type IIA (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378269018 Osteogenesis imperfecta type IIA en Synonym Active Initial character case insensitive SNOMED CT core
378270017 Osteogenesis imperfecta congenita neonatal lethal form en Synonym Active Case insensitive SNOMED CT core
378271018 Osteogenesis imperfecta, neonatal lethal en Synonym Active Case insensitive SNOMED CT core
644956016 Osteogenesis imperfecta type IIA (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4694544011 Osteogenesis imperfecta type IIA presents with broad ribs with multiple fractures, continuous beaded ribs and severe under-modeling of the femur. en Definition Active Case sensitive SNOMED CT core
4694545012 Osteogenesis imperfecta type IIA presents with broad ribs with multiple fractures, continuous beaded ribs and severe under-modelling of the femur. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta type IIA Occurrence Congenital true Inferred relationship Some 1
Osteogenesis imperfecta type IIA Pathological process Pathological developmental process true Inferred relationship Some 1
Osteogenesis imperfecta type IIA Has interpretation Abnormal true Inferred relationship Some 2
Osteogenesis imperfecta type IIA Interprets Bone formation true Inferred relationship Some 2
Osteogenesis imperfecta type IIA Associated morphology Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta type IIA Associated morphology Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta type IIA Finding site Bone structure false Inferred relationship Some 1
Osteogenesis imperfecta type IIA Occurrence Congenital false Inferred relationship Some 2
Osteogenesis imperfecta type IIA Finding site Bone structure false Inferred relationship Some 2
Osteogenesis imperfecta type IIA Associated morphology Congenital dysplasia false Inferred relationship Some 2
Osteogenesis imperfecta type IIA Finding site Connective tissue structure false Inferred relationship Some
Osteogenesis imperfecta type IIA Associated morphology Dysplasia true Inferred relationship Some 1
Osteogenesis imperfecta type IIA Finding site Skeletal system structure false Inferred relationship Some 1
Osteogenesis imperfecta type IIA Occurrence Congenital false Inferred relationship Some
Osteogenesis imperfecta type IIA Finding site Connective tissue false Inferred relationship Some
Osteogenesis imperfecta type IIA Finding site Bone structure true Inferred relationship Some 1
Osteogenesis imperfecta type IIA Is a Osteogenesis imperfecta, perinatal lethal true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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