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1286833006: Spondyloepimetaphyseal dysplasia with joint laxity Beighton type (disorder)


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


0 descendants.

Expanded Value Set


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)

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