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 |
378212017 | Autosomal recessive spondyloepimetaphyseal dysplasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
644903018 | Autosomal recessive spondyloepimetaphyseal dysplasia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spondyloepimetaphyseal dysplasia | Is a | Osteochondrodysplasia syndrome | false | Inferred relationship | Some | ||
Autosomal recessive spondyloepimetaphyseal dysplasia | Is a | Spondyloepimetaphyseal disorder | false | Inferred relationship | Some | ||
Autosomal recessive spondyloepimetaphyseal dysplasia | Associated morphology | Dysplasia | false | Inferred relationship | Some | 1 | |
Autosomal recessive spondyloepimetaphyseal dysplasia | Finding site | Skeletal system structure | false | Inferred relationship | Some | 1 | |
Autosomal recessive spondyloepimetaphyseal dysplasia | Finding site | Bone structure | false | Inferred relationship | Some | 1 | |
Autosomal recessive spondyloepimetaphyseal dysplasia | Occurrence | Congenital | false | Inferred relationship | Some | ||
Autosomal recessive spondyloepimetaphyseal dysplasia | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Autosomal recessive spondyloepimetaphyseal dysplasia | Associated morphology | Congenital malformation | false | Inferred relationship | Some | ||
Autosomal recessive spondyloepimetaphyseal dysplasia | Finding site | Bone structure | false | Inferred relationship | Some | 1 | |
Autosomal recessive spondyloepimetaphyseal dysplasia | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Autosomal recessive spondyloepimetaphyseal dysplasia | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Autosomal recessive spondyloepimetaphyseal dysplasia | Finding site | Bone structure | false | Inferred relationship | Some | 2 | |
Autosomal recessive spondyloepimetaphyseal dysplasia | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Spondyloepimetaphyseal dysplasia Irapa type (disorder) | Is a | False | Autosomal recessive spondyloepimetaphyseal dysplasia | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)