Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3465115018 | Marfanoid syndrome De Silva type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3465116017 | Marfanoid syndrome De Silva type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3465117014 | Syndrome that is characterized by the association of marfanoid habitus with visceral diverticula. It has been reported in four adults and two siblings from a consanguineous marriage in two different publications. Pediatric cases also presented with diaphragmatic hernia. Other connective tissue disorders with visceral diverticula have been reported previously, suggesting a relationship between these two conditions. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3465118016 | Syndrome that is characterised by the association of marfanoid habitus with visceral diverticula. It has been reported in four adults and two siblings from a consanguineous marriage in two different publications. Paediatric cases also presented with diaphragmatic hernia. Other connective tissue disorders with visceral diverticula have been reported previously, suggesting a relationship between these two conditions. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
1014481000172116 | syndrome marfanoïde type de Silva | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Marfanoid syndrome De Silva type (disorder) | Is a | Hereditary disease | false | Inferred relationship | Some | ||
Marfanoid syndrome De Silva type (disorder) | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
Marfanoid syndrome De Silva type (disorder) | Is a | trouble selon la localisation corporelle | false | Inferred relationship | Some | ||
Marfanoid syndrome De Silva type (disorder) | Is a | Marfanoid physique | true | Inferred relationship | Some | ||
Marfanoid syndrome De Silva type (disorder) | Is a | Viscus structure finding (finding) | true | Inferred relationship | Some | ||
Marfanoid syndrome De Silva type (disorder) | Interprets | Physique type | true | Inferred relationship | Some | 2 | |
Marfanoid syndrome De Silva type (disorder) | Associated morphology | Congenital diverticulum | false | Inferred relationship | Some | 3 | |
Marfanoid syndrome De Silva type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Marfanoid syndrome De Silva type (disorder) | Finding site | Structure of viscus | false | Inferred relationship | Some | 3 | |
Marfanoid syndrome De Silva type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Marfanoid syndrome De Silva type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Marfanoid syndrome De Silva type (disorder) | Associated morphology | Congenital diverticulum | true | Inferred relationship | Some | 1 | |
Marfanoid syndrome De Silva type (disorder) | Finding site | Structure of viscus | true | Inferred relationship | Some | 1 | |
Marfanoid syndrome De Silva type (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets