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279309008: Osteogenesis imperfecta, type IV B (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta, type IV B Is a Osteogenesis imperfecta type IV true Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV B Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV B Occurrence Congenital false Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV B Finding site Connective tissue structure false Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV B Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV B Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV B Finding site Connective tissue false Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV B Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV B Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV B Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV B Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, type IV B Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, type IV B Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, type IV B Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV B Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Osteogenesis imperfecta, type IV B Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, type IV B Interprets Bone formation, function true Inferred relationship Existential restriction modifier 2
Osteogenesis imperfecta, type IV B Is a Dentinogenesis imperfecta true Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV B Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV B Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Osteogenesis imperfecta, type IV B Finding site Dentin structure true Inferred relationship Existential restriction modifier 3
Osteogenesis imperfecta, type IV B Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Osteogenesis imperfecta, type IV B Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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