Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3304330019 | Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304331015 | Camptodactyly with joint contracture and facial skeletal defect syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3304332010 | Rozin Hertz Goodman syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3304333017 | Rozin camptodactyly syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3304334011 | The association of camptodactyly, multiple eye defects (fibrosis of the medial rectus muscle, severe myopia, ptosis and exophthalmos), scoliosis, flexion contractures and facial anomalies (arched eyebrows, facial asymmetry with an abnormal skull shape, a prominent nose, small mouth, low-set and dysplastic ears, and a low nuchal hairline). Only four cases have been reported in the literature so far. The mode of inheritance remains to be confirmed, but both autosomal dominant and recessive transmission have been considered. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
932041000172113 | syndrome de camptodactylie-raideur articulaire-anomalies osseuses de la face | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
990161000172115 | syndrome de Rozin-Hertz-Goodman | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
900281000172115 | syndroom van Rozin-camptodactylie | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
902461000172110 | camptodactylie, gewrichtscontracturen, faciale skeletale defecten-syndroom | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Is a | Camptodactyly | true | Inferred relationship | Some | ||
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Is a | Arthrogryposis | false | Inferred relationship | Some | ||
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Flexion deformity | false | Inferred relationship | Some | 4 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Musculoskeletal structure of digit of hand | false | Inferred relationship | Some | 4 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 6 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 7 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 7 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 4 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 6 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Face structure | false | Inferred relationship | Some | 6 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Finger structure | false | Inferred relationship | Some | 7 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Contracture | false | Inferred relationship | Some | 5 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 5 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | false | Inferred relationship | Some | 3 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Finger structure | false | Inferred relationship | Some | 3 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Musculoskeletal structure of digit of hand | false | Inferred relationship | Some | 2 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Flexion deformity | false | Inferred relationship | Some | 2 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Contracture | false | Inferred relationship | Some | 1 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Is a | Congenital anomaly of joint | false | Inferred relationship | Some | ||
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 3 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 4 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Joint structure | false | Inferred relationship | Some | 1 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Interprets | Range of joint movement | true | Inferred relationship | Some | 3 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Has interpretation | Decreased | true | Inferred relationship | Some | 3 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Structure of joint region | true | Inferred relationship | Some | 1 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Fixed flexion deformity (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Finding site | Musculoskeletal system structure of digit (body structure) | true | Inferred relationship | Some | 2 | |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Is a | Flexion contracture | true | Inferred relationship | Some | ||
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) | Associated morphology | Flexion contracture | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets