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254068007: Opsismodysplasia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
378220015 Opsismodysplasia en Synonym Active Case insensitive SNOMED CT core
644909019 Opsismodysplasia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Opsismodysplasia Pathological process Pathological developmental process true Inferred relationship Some 1
Opsismodysplasia Occurrence Congenital true Inferred relationship Some 1
Opsismodysplasia Interprets Height / growth measure true Inferred relationship Some 2
Opsismodysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 1
Opsismodysplasia Finding site Bone structure false Inferred relationship Some 1
Opsismodysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 1
Opsismodysplasia Associated morphology Dysplasia true Inferred relationship Some 1
Opsismodysplasia Finding site Skeletal system structure false Inferred relationship Some 1
Opsismodysplasia Occurrence Congenital false Inferred relationship Some 2
Opsismodysplasia Finding site Bone structure false Inferred relationship Some 2
Opsismodysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 2
Opsismodysplasia Finding site Bone structure true Inferred relationship Some 1
Opsismodysplasia Occurrence Congenital false Inferred relationship Some
Opsismodysplasia Is a Spondyloepimetaphyseal disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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