FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

205497004: Osteogenesis imperfecta type IV (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
315124015 Osteogenesis imperfecta type IV en Synonym Active Initial character case insensitive SNOMED CT core
315125019 Osteogenesis imperfecta, type IV en Synonym Active Initial character case insensitive SNOMED CT core
315126018 Osteogenesis imperfecta with normal sclerae, dominant form en Synonym Active Case insensitive SNOMED CT core
590872019 Osteogenesis imperfecta type IV (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Osteogenesis imperfecta with normal sclerae, dominant form Occurrence Congenital true Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Pathological process 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
Osteogenesis imperfecta with normal sclerae, dominant form Associated morphology Congenital dysplasia false Inferred relationship Some 1
Osteogenesis imperfecta with normal sclerae, dominant form Is a Osteogenesis imperfecta true Inferred relationship Some
Osteogenesis imperfecta with normal sclerae, dominant form Associated morphology Congenital dysplasia 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 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 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 Congenital dysplasia false 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 Is a True Osteogenesis imperfecta with normal sclerae, dominant form Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Back to Start