Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3315249017 | Spondyloepimetaphyseal dysplasia Missouri type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3315250017 | Spondyloepimetaphyseal dysplasia Missouri type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3315251018 | Spondyloepimetaphyseal dysplasia type 2 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3315252013 | Disorder with manifestations of moderate-to-severe metaphyseal changes, mild epiphyseal involvement, rhizomelic shortening of the lower limbs with bowing of the femora and/or tibiae, coxa vara, genu varum and pear-shaped vertebrae in childhood. The syndrome has been described in a large Missouri (US) kindred with 14 affected members in 4 generations. Though some spontaneous improvement of the skeletal defects may occur in adolescence, the affected individuals remained shorter than their age-matched unaffected siblings. Predisposition deformities to osteoarthritis have been noted. This condition is caused by mutation in the MMP13 gene (locus 11q22.3) and transmitted in an autosomal dominant manner. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Spondyloepimetaphyseal dysplasia Missouri type | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia Missouri type | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia Missouri type | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia Missouri type | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia Missouri type | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Spondyloepimetaphyseal dysplasia Missouri type | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia Missouri type | Interprets | Height / growth measure | true | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia Missouri type | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia Missouri type | Is a | Spondyloepimetaphyseal disorder | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia Missouri type | Is a | Inherited disorder of connective tissue | false | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia Missouri type | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Spondyloepimetaphyseal dysplasia Missouri type | Associated morphology | Congenital dysplasia | false | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia Missouri type | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Spondyloepimetaphyseal dysplasia Missouri type | Finding site | Bone structure | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set