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279309008: Osteogenesis imperfecta, type IV B (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
416527010 Osteogenesis imperfecta, type IV B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4694693011 Osteogenesis imperfecta type IV with dentinogenesis imperfecta en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
672578011 Osteogenesis imperfecta, type IV B (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta, type IV B Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteogenesis imperfecta, type IV B survenue (attribut) congénital true Inferred relationship Some 1
Osteogenesis imperfecta, type IV B a pour interprétation (attribut) anormal true Inferred relationship Some 2
Osteogenesis imperfecta, type IV B interprète (attribut) Bone formation, function (observable entity) true Inferred relationship Some 2
Osteogenesis imperfecta, type IV B est un(e) (attribut) Dentinogenesis imperfecta true Inferred relationship Some
Osteogenesis imperfecta, type IV B est un(e) (attribut) Hereditary disorder of musculoskeletal system true Inferred relationship Some
Osteogenesis imperfecta, type IV B survenue (attribut) congénital true Inferred relationship Some 3
Osteogenesis imperfecta, type IV B localisation d'une constatation (attribut) Dentin structure true Inferred relationship Some 3
Osteogenesis imperfecta, type IV B morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 3
Osteogenesis imperfecta, type IV B Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Osteogenesis imperfecta, type IV B morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta, type IV B localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 1
Osteogenesis imperfecta, type IV B morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta, type IV B survenue (attribut) congénital false Inferred relationship Some 2
Osteogenesis imperfecta, type IV B localisation d'une constatation (attribut) structure osseuse false Inferred relationship Some 2
Osteogenesis imperfecta, type IV B morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 2
Osteogenesis imperfecta, type IV B localisation d'une constatation (attribut) Skeletal system structure false Inferred relationship Some 1
Osteogenesis imperfecta, type IV B survenue (attribut) congénital false Inferred relationship Some
Osteogenesis imperfecta, type IV B localisation d'une constatation (attribut) Connective tissue structure false Inferred relationship Some
Osteogenesis imperfecta, type IV B morphologie associée (attribut) dysplasie true Inferred relationship Some 1
Osteogenesis imperfecta, type IV B localisation d'une constatation (attribut) structure osseuse true Inferred relationship Some 1
Osteogenesis imperfecta, type IV B localisation d'une constatation (attribut) Connective tissue false Inferred relationship Some
Osteogenesis imperfecta, type IV B est un(e) (attribut) Osteogenesis imperfecta with normal sclerae, dominant form true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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