702350003: Spondyloepimetaphyseal dysplasia, Strudwick type (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \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\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\Multiple system malformation syndrome\Osteochondrodysplasia syndrome\Spondyloepimetaphyseal dysplasia, Strudwick type

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2995130013	Dappled metaphysis syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3008581017	Spondyloepimetaphyseal dysplasia, Strudwick type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3008635013	Spondyloepimetaphyseal dysplasia, Strudwick type (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3008691019	SEMD - spondyloepimetaphyseal dysplasia, Strudwick type	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3008722011	Strudwick syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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