254063003: Autosomal recessive spondyloepimetaphyseal dysplasia (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module	Reference Sets
378212017	Autosomal recessive spondyloepimetaphyseal dysplasia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	Description inactivation indicator reference set: Concept non-current
644903018	Autosomal recessive spondyloepimetaphyseal dysplasia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	Description inactivation indicator reference set: Concept non-current
1996471000052111	autosomal recessiv spondyloepimetafyseal dysplasi	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)	Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
autosomal recessiv spondyloepimetafyseal dysplasi	Is a	Osteochondrodysplasia syndrome	false	Inferred relationship	Some
autosomal recessiv spondyloepimetafyseal dysplasi	Is a	Spondyloepimetaphyseal disorder	false	Inferred relationship	Some
autosomal recessiv spondyloepimetafyseal dysplasi	Associated morphology	Dysplasia	false	Inferred relationship	Some	1
autosomal recessiv spondyloepimetafyseal dysplasi	Finding site	Skeletal system structure	false	Inferred relationship	Some	1
autosomal recessiv spondyloepimetafyseal dysplasi	Finding site	Bone structure	false	Inferred relationship	Some	1
autosomal recessiv spondyloepimetafyseal dysplasi	Occurrence	Congenital	false	Inferred relationship	Some
autosomal recessiv spondyloepimetafyseal dysplasi	Associated morphology	kongenital dysplasi	false	Inferred relationship	Some	1
autosomal recessiv spondyloepimetafyseal dysplasi	Associated morphology	medfödd missbildning	false	Inferred relationship	Some
autosomal recessiv spondyloepimetafyseal dysplasi	Finding site	Bone structure	false	Inferred relationship	Some	1
autosomal recessiv spondyloepimetafyseal dysplasi	Associated morphology	kongenital dysplasi	false	Inferred relationship	Some	1
autosomal recessiv spondyloepimetafyseal dysplasi	Occurrence	Congenital	false	Inferred relationship	Some	2
autosomal recessiv spondyloepimetafyseal dysplasi	Finding site	Bone structure	false	Inferred relationship	Some	2
autosomal recessiv spondyloepimetafyseal dysplasi	Associated morphology	kongenital dysplasi	false	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Spondyloepimetaphyseal dysplasia Irapa type (disorder)	Is a	False	autosomal recessiv spondyloepimetafyseal dysplasi	Inferred relationship	Some

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)