Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3755744018 | Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3755745017 | Autosomal recessive spondylometaphyseal dysplasia Megarbane type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3755746016 | A rare primary bone dysplasia with characteristics of intrauterine growth retardation, pre and postnatal disproportionate short stature with short, rhizomelic limbs, facial dysmorphism, a short neck and small thorax. Hypotonia, cardiomegaly and global developmental delay have also been associated. Several radiographic findings have been reported, including ribs with cupped ends, platyspondyly, square iliac bones, horizontal and trident acetabula, hypoplastic ischia, and delayed epiphyseal ossification. There is evidence this disease is caused by homozygous mutation in the MAGMAS (PAM16) gene on chromosome 16p13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4352151000052118 | autosomalt recessiv spondylometafyseal dysplasi, Megarbane-typ | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Finding site | Bone structure | false | Inferred relationship | Some | 1 | |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Is a | Spondylometaphyseal dysplasia | true | Inferred relationship | Some | ||
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Is a | Congenital anomaly of skeletal bone | false | Inferred relationship | Some | ||
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Is a | Rhizomelic dysplasia (disorder) | true | Inferred relationship | Some | ||
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Interprets | Limb length | true | Inferred relationship | Some | 2 | |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 2 | |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Finding site | Bone structure of extremity | true | Inferred relationship | Some | 1 | |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Is a | Short stature disorder | true | Inferred relationship | Some | ||
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Interprets | Body height measure (observable entity) | true | Inferred relationship | Some | 3 | |
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets