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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
672578011 Osteogenesis imperfecta, type IV B (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
837951000052112 osteogenesis imperfecta, typ 4 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 IV B Is a Osteogenesis imperfecta with normal sclerae, dominant form true Inferred relationship Some
Osteogenesis imperfecta, type IV B Finding site Skeletal system structure false Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Occurrence Congenital false Inferred relationship Some
Osteogenesis imperfecta, type IV B Finding site Connective tissue structure false Inferred relationship Some
Osteogenesis imperfecta, type IV B Associated morphology Dysplasia true Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Finding site Bone structure true Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Finding site Connective tissue false Inferred relationship Some
Osteogenesis imperfecta, type IV B Associated morphology kongenital dysplasi false Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Finding site Bone structure false Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Associated morphology kongenital dysplasi false Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Occurrence Congenital false Inferred relationship Some 2
Osteogenesis imperfecta, type IV B Finding site Bone structure false Inferred relationship Some 2
Osteogenesis imperfecta, type IV B Associated morphology kongenital dysplasi false Inferred relationship Some 2
Osteogenesis imperfecta, type IV B Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Occurrence Congenital true Inferred relationship Some 1
Osteogenesis imperfecta, type IV B Has interpretation Abnormal true Inferred relationship Some 2
Osteogenesis imperfecta, type IV B 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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