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205497004: Osteogenesis imperfecta type IV (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
315124015 Osteogenesis imperfecta type IV en Synonym Active Only initial character case insensitive SNOMED CT core module
315125019 Osteogenesis imperfecta, type IV en Synonym Active Only initial character case insensitive SNOMED CT core module
315126018 Osteogenesis imperfecta with normal sclerae, dominant form en Synonym Active Entire term case insensitive SNOMED CT core module
590872019 Osteogenesis imperfecta type IV (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Osteogenesis imperfecta, type IV B Is a True Osteogenesis imperfecta type IV Inferred relationship Existential restriction modifier
Osteogenesis imperfecta, type IV A Is a True Osteogenesis imperfecta type IV Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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