702350003: Spondyloepimetaphyseal dysplasia, Strudwick type (disorder)

SNOMED CT Concept\constatation clinique\Disease\...

\Genetic disease\maladie héréditaire\...

\Developmental hereditary disorder\Spondyloepimetaphyseal dysplasia, Strudwick type

\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Spondyloepimetaphyseal dysplasia, Strudwick type

\Congenital disease\Congenital malformation\Congenital malformation syndrome (disorder)\syndrome de malformations multisystémiques\Osteochondrodysplasia syndrome\Spondyloepimetaphyseal dysplasia, Strudwick type

\trouble du développement\Developmental hereditary disorder\Spondyloepimetaphyseal dysplasia, Strudwick type
\trouble du développement\Congenital malformation\Congenital malformation syndrome (disorder)\syndrome de malformations multisystémiques\Osteochondrodysplasia syndrome\Spondyloepimetaphyseal dysplasia, Strudwick type

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2995130013 Dappled metaphysis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3008581017 Spondyloepimetaphyseal dysplasia, Strudwick type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3008635013 Spondyloepimetaphyseal dysplasia, Strudwick type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3008691019 SEMD - spondyloepimetaphyseal dysplasia, Strudwick type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3008722011 Strudwick syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Spondyloepimetaphyseal dysplasia, Strudwick type	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia, Strudwick type	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia, Strudwick type	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
Spondyloepimetaphyseal dysplasia, Strudwick type	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Spondyloepimetaphyseal dysplasia, Strudwick type	est un(e) (attribut)	Osteochondrodysplasia syndrome	true	Inferred relationship	Some
Spondyloepimetaphyseal dysplasia, Strudwick type	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia, Strudwick type	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Canada English language reference set (foundation metadata concept)