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254111008: Osteogenesis imperfecta type IIB (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
378272013 Osteogenesis imperfecta type IIB en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
644957013 Osteogenesis imperfecta type IIB (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
837891000052110 osteogenesis imperfecta, typ 2 B 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 IIB Is a Osteogenesis imperfecta, perinatal lethal true Inferred relationship Some
Osteogenesis imperfecta type IIB Is a Osteogenesis imperfecta, perinatal lethal (disorder) false Inferred relationship Some
Osteogenesis imperfecta type IIB Associated morphology Dysplasia true Inferred relationship Some 1
Osteogenesis imperfecta type IIB Finding site Skeletal system structure false Inferred relationship Some 1
Osteogenesis imperfecta type IIB Finding site Bone structure true Inferred relationship Some 1
Osteogenesis imperfecta type IIB Finding site Connective tissue false Inferred relationship Some
Osteogenesis imperfecta type IIB Occurrence Congenital false Inferred relationship Some
Osteogenesis imperfecta type IIB Finding site Connective tissue structure false Inferred relationship Some
Osteogenesis imperfecta type IIB Associated morphology kongenital dysplasi false Inferred relationship Some 1
Osteogenesis imperfecta type IIB Associated morphology kongenital dysplasi false Inferred relationship Some 1
Osteogenesis imperfecta type IIB Finding site Bone structure false Inferred relationship Some 1
Osteogenesis imperfecta type IIB Occurrence Congenital false Inferred relationship Some 2
Osteogenesis imperfecta type IIB Finding site Bone structure false Inferred relationship Some 2
Osteogenesis imperfecta type IIB Associated morphology kongenital dysplasi false Inferred relationship Some 2
Osteogenesis imperfecta type IIB Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteogenesis imperfecta type IIB Occurrence Congenital true Inferred relationship Some 1
Osteogenesis imperfecta type IIB Has interpretation Abnormal true Inferred relationship Some 2
Osteogenesis imperfecta type IIB 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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