Status: current, 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 |
3315232012 | Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3315233019 | Spondyloepimetaphyseal dysplasia matrilin-3 type | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401989018 | A rare primary bone dysplasia due to matrilin-3 variants and characterized by disproportionate early-onset dwarfism, bowing of the lower limbs, short, wide and stocky long bones with severe epiphyseal and metaphyseal changes, lumbar lordosis, hypoplastic iliac bones, flat ovoid vertebral bodies and normal hands. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401990010 | A rare primary bone dysplasia due to matrilin-3 variants and characterised by disproportionate early-onset dwarfism, bowing of the lower limbs, short, wide and stocky long bones with severe epiphyseal and metaphyseal changes, lumbar lordosis, hypoplastic iliac bones, flat ovoid vertebral bodies and normal hands. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Is a | Spondyloepimetaphyseal disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Finding site | Bone structure | false | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia matrilin-3 type (disorder) | Interprets | Height / growth measure | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)