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280159008: Osteogenesis imperfecta, type IV A (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
417688018 Osteogenesis imperfecta, type IV A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
673534011 Osteogenesis imperfecta, type IV A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4694694017 Osteogenesis imperfecta type IV with normal teeth en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
837941000052114 osteogenesis imperfecta, typ 4 A sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta, type IV A (disorder) Is a Osteogenesis imperfecta with normal sclerae, dominant form true Inferred relationship Some
Osteogenesis imperfecta, type IV A (disorder) Finding site Bone structure true Inferred relationship Some 1
Osteogenesis imperfecta, type IV A (disorder) Finding site Connective tissue structure false Inferred relationship Some
Osteogenesis imperfecta, type IV A (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Osteogenesis imperfecta, type IV A (disorder) Finding site Skeletal system structure false Inferred relationship Some 1
Osteogenesis imperfecta, type IV A (disorder) Occurrence Congenital false Inferred relationship Some
Osteogenesis imperfecta, type IV A (disorder) Finding site Connective tissue false Inferred relationship Some
Osteogenesis imperfecta, type IV A (disorder) Associated morphology kongenital dysplasi false Inferred relationship Some 1
Osteogenesis imperfecta, type IV A (disorder) Associated morphology kongenital dysplasi false Inferred relationship Some 1
Osteogenesis imperfecta, type IV A (disorder) Finding site Bone structure false Inferred relationship Some 1
Osteogenesis imperfecta, type IV A (disorder) Occurrence Congenital false Inferred relationship Some 2
Osteogenesis imperfecta, type IV A (disorder) Finding site Bone structure false Inferred relationship Some 2
Osteogenesis imperfecta, type IV A (disorder) Associated morphology kongenital dysplasi false Inferred relationship Some 2
Osteogenesis imperfecta, type IV A (disorder) Occurrence Congenital true Inferred relationship Some 1
Osteogenesis imperfecta, type IV A (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteogenesis imperfecta, type IV A (disorder) Has interpretation Abnormal true Inferred relationship Some 2
Osteogenesis imperfecta, type IV A (disorder) Interprets Bone formation true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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