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1197018005: Osteogenesis imperfecta type IIC (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4694534014 Osteogenesis imperfecta type IIC (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4694535010 Osteogenesis imperfecta type IIC en Synonym Active Only initial character case insensitive SNOMED CT core module
4694537019 Lethal osteogenesis imperfecta with thin long bones and thin and beaded ribs en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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