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279309008: Osteogenesis imperfecta, type IV B (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
416527010 Osteogenesis imperfecta, type IV B en Synonym Active Initial character case insensitive SNOMED CT core
4694693011 Osteogenesis imperfecta type IV with dentinogenesis imperfecta en Synonym Active Initial character case insensitive SNOMED CT core
672578011 Osteogenesis imperfecta, type IV B (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta, type IV B Pathological process 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
Osteogenesis imperfecta, type IV B Is a Dentinogenesis imperfecta true Inferred relationship Some
Osteogenesis imperfecta, type IV B Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Osteogenesis imperfecta, type IV B Occurrence Congenital true Inferred relationship Some 3
Osteogenesis imperfecta, type IV B Finding site Dentin structure true Inferred relationship Some 3
Osteogenesis imperfecta, type IV B Associated morphology Morphologically abnormal structure true Inferred relationship Some 3
Osteogenesis imperfecta, type IV B Pathological process Pathological developmental process true Inferred relationship Some 3
Osteogenesis imperfecta, type IV B Associated morphology Congenital dysplasia 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 Congenital dysplasia 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 Congenital dysplasia false Inferred relationship Some 2
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 Is a Osteogenesis imperfecta with normal sclerae, dominant form true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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