Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2023. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5255575016 | Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5255576015 | Spondyloepimetaphyseal dysplasia with joint laxity Beighton type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5255577012 | SEMDJL1 - spondyloepimetaphyseal dysplasia with joint laxity type 1 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5255583010 | Spondyloepimetaphyseal dysplasia with joint laxity type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5400760019 | A rare primary bone dysplasia with multiple joint dislocations characterized by stunted stature, articular hypermobility and spinal malalignment resulting in severe progressive kyphosis. Joint dislocations include bilateral dislocation of the radial heads with elbow contractures, feet (bilateral talipes equinovarus) and congenital dislocations of the hip and genu valgus. Joint laxity is particularly observed in fingers. Spinal changes include moderate platyspondyly with anterior projection of the vertebral bodies. Facial features of oval face with a flattened nasal bridge, button nose, long upper lip, prominent eyes and blue sclera are characteristic but variable. Patients may also present mild skin extensibility, spatulate terminal phalanges, lip and palate clefts, micrognathia and structural cardiac malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400761015 | A rare primary bone dysplasia with multiple joint dislocations characterised by stunted stature, articular hypermobility and spinal malalignment resulting in severe progressive kyphosis. Joint dislocations include bilateral dislocation of the radial heads with elbow contractures, feet (bilateral talipes equinovarus) and congenital dislocations of the hip and genu valgus. Joint laxity is particularly observed in fingers. Spinal changes include moderate platyspondyly with anterior projection of the vertebral bodies. Facial features of oval face with a flattened nasal bridge, button nose, long upper lip, prominent eyes and blue sclera are characteristic but variable. Patients may also present mild skin extensibility, spatulate terminal phalanges, lip and palate clefts, micrognathia and structural cardiac malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Spondyloepimetaphyseal disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Range of joint movement increased (finding) | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Joint laxity | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Finding of vertebra | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Chronic arthropathy | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Movement disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Disorder of vertebral column (disorder) | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Congenital anomaly of spine | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 5 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Interprets | Body height measure (observable entity) | true | Inferred relationship | Some | 3 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Has interpretation | Below reference range | true | Inferred relationship | Some | 3 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Interprets | Range of joint movement | true | Inferred relationship | Some | 4 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Has interpretation | Increased | true | Inferred relationship | Some | 4 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Finding site | Bone structure of vertebra | true | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type | Finding site | Joint structure | true | Inferred relationship | Some | 6 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)