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254110009: Osteogenesis imperfecta type IIA (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378269018 Osteogenesis imperfecta type IIA en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378270017 Osteogenesis imperfecta congenita neonatal lethal form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
378271018 Osteogenesis imperfecta, neonatal lethal en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644956016 Osteogenesis imperfecta type IIA (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta type IIA survenue (attribut) congénital true Inferred relationship Some 1
Osteogenesis imperfecta type IIA Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteogenesis imperfecta type IIA a pour interprétation (attribut) anormal true Inferred relationship Some 2
Osteogenesis imperfecta type IIA interprète (attribut) Bone formation, function (observable entity) true Inferred relationship Some 2
Osteogenesis imperfecta type IIA morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta type IIA morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta type IIA localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 1
Osteogenesis imperfecta type IIA survenue (attribut) congénital false Inferred relationship Some 2
Osteogenesis imperfecta type IIA localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 2
Osteogenesis imperfecta type IIA morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 2
Osteogenesis imperfecta type IIA localisation d'une constatation (attribut) Connective tissue structure false Inferred relationship Some
Osteogenesis imperfecta type IIA morphologie associée (attribut) dysplasie true Inferred relationship Some 1
Osteogenesis imperfecta type IIA localisation d'une constatation (attribut) Skeletal system structure false Inferred relationship Some 1
Osteogenesis imperfecta type IIA survenue (attribut) congénital false Inferred relationship Some
Osteogenesis imperfecta type IIA localisation d'une constatation (attribut) Connective tissue false Inferred relationship Some
Osteogenesis imperfecta type IIA localisation d'une constatation (attribut) structure osseuse true Inferred relationship Some 1
Osteogenesis imperfecta type IIA est un(e) (attribut) Osteogenesis imperfecta, perinatal lethal true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada French language reference set (foundation metadata concept)

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