Status: current, 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 |
3705361012 | Autosomal dominant multiple pterygium syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3705362017 | Distal arthrogryposis type 8 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3705363010 | Autosomal dominant multiple pterygium syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3705364016 | A rare distal arthrogryposis syndrome with characteristics of multiple pterygia (typically involving the neck, axilla and popliteal areas), joint contractures, ptosis, camptodactyly of the hands with hypoplastic flexion creases, vertebral fusions, severe scoliosis and short stature. There is evidence this disease is caused by heterozygous mutation in the MYH3 gene on chromosome 17p13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant multiple pterygium syndrome (disorder) | Is a | Distal arthrogryposis syndrome | true | Inferred relationship | Some | ||
Autosomal dominant multiple pterygium syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant multiple pterygium syndrome (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 1 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Finding site | Joint structure of limb | false | Inferred relationship | Some | 1 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Is a | Multiple pterygium syndrome | true | Inferred relationship | Some | ||
Autosomal dominant multiple pterygium syndrome (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 2 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Interprets | Range of joint movement | true | Inferred relationship | Some | 2 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Associated morphology | Congenital webbing | true | Inferred relationship | Some | 3 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Finding site | Structure of joint region | true | Inferred relationship | Some | 1 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 3 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Is a | Inherited arthrogryposis | true | Inferred relationship | Some | ||
Autosomal dominant multiple pterygium syndrome (disorder) | Finding site | Joint structure of multiple body sites (body structure) | true | Inferred relationship | Some | 4 | |
Autosomal dominant multiple pterygium syndrome (disorder) | Associated morphology | Contracture | true | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets