702350003: Spondyloepimetaphyseal dysplasia, Strudwick type (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\...

\Developmental hereditary disorder\Spondyloepimetaphyseal dysplasia, Strudwick type

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

\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Osteochondrodysplasia syndrome\Spondyloepimetaphyseal dysplasia, Strudwick type

\Developmental disorder\Developmental hereditary disorder\Spondyloepimetaphyseal dysplasia, Strudwick type
\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\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	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Spondyloepimetaphyseal dysplasia, Strudwick type	Is a	Osteochondrodysplasia syndrome	true	Inferred relationship	Some
Spondyloepimetaphyseal dysplasia, Strudwick type	Occurrence	Congenital	true	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia, Strudwick type	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia, Strudwick type	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia, Strudwick type	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Spondyloepimetaphyseal dysplasia, Strudwick type	Is a	Developmental hereditary disorder	true	Inferred relationship	Some

Inbound Relationships

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Reference Sets

Description inactivation indicator reference set