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205497004: Osteogenesis imperfecta type IV (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
315124015 Osteogenesis imperfecta type IV en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315125019 Osteogenesis imperfecta, type IV en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315126018 Osteogenesis imperfecta with normal sclerae, dominant form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
590872019 Osteogenesis imperfecta type IV (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3645901000052118 osteogenesis imperfecta med normal senhinna, dominant form sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta with normal sclerae, dominant form Is a Osteogenesis imperfecta true Inferred relationship Some
Osteogenesis imperfecta with normal sclerae, dominant form Finding site Skeletal system structure false Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Occurrence Congenital false Inferred relationship Some
Osteogenesis imperfecta with normal sclerae, dominant form Finding site Connective tissue false Inferred relationship Some
Osteogenesis imperfecta with normal sclerae, dominant form Finding site Bone structure true Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Associated morphology Dysplasia true Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Finding site Connective tissue structure false Inferred relationship Some
Osteogenesis imperfecta with normal sclerae, dominant form Associated morphology kongenital dysplasi false Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Associated morphology kongenital dysplasi false Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Finding site Bone structure false Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Occurrence Congenital false Inferred relationship Some 2
Osteogenesis imperfecta with normal sclerae, dominant form Finding site Bone structure false Inferred relationship Some 2
Osteogenesis imperfecta with normal sclerae, dominant form Associated morphology kongenital dysplasi false Inferred relationship Some 2
Osteogenesis imperfecta with normal sclerae, dominant form Occurrence Congenital true Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Has interpretation Abnormal true Inferred relationship Some 2
Osteogenesis imperfecta with normal sclerae, dominant form Interprets Bone formation true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Osteogenesis imperfecta, type IV B Is a True Osteogenesis imperfecta with normal sclerae, dominant form Inferred relationship Some
Osteogenesis imperfecta, type IV A (disorder) Is a True Osteogenesis imperfecta with normal sclerae, dominant form Inferred relationship Some

This concept is not in any reference sets

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