Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4970633011 | Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4970634017 | Cutaneovisceral angiomatosis, thrombocytopenia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4970635016 | MLT - multifocal lymphangioendotheliomatosis with thrombocytopenia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4970636015 | Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4970637012 | A rare lymphatic system anomaly with characteristics of multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically the lesions appear as round to oval red-brown plaques and as large as a few centimeters in diameter. Histopathologically they consist of dilated thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers and resembling benign lymphangioendothelioma. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4970638019 | A rare lymphatic system anomaly with characteristics of multifocal congenital and progressive vascular lesions of the skin, gastrointestinal tract and occasionally other anatomic sites, causing potentially life-threatening thrombocytopenic coagulopathy. Macroscopically the lesions appear as round to oval red-brown plaques and as large as a few centimetres in diameter. Histopathologically they consist of dilated thin-walled vessels with variable endothelial hyperplasia, positive for lymphatic endothelial cell markers and resembling benign lymphangioendothelioma. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | est un(e) (attribut) | Lymphatic malformation | true | Inferred relationship | Some | ||
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | est un(e) (attribut) | constatation à propos d'un lymphonoeud et des lymphatiques | true | Inferred relationship | Some | ||
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | est un(e) (attribut) | Congenital thrombocytopenia (disorder) | true | Inferred relationship | Some | ||
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | interprète (attribut) | Hemostatic function (observable entity) | true | Inferred relationship | Some | 2 | |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 2 | |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | interprète (attribut) | Platelet count | true | Inferred relationship | Some | 3 | |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | a pour interprétation (attribut) | au-dessous de l'étendue de référence | true | Inferred relationship | Some | 3 | |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | localisation d'une constatation (attribut) | vaisseau lymphatique | true | Inferred relationship | Some | 1 | |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | morphologie associée (attribut) | Congenital lymphatic malformation (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR