Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
350519013 | Pulmonary capillary haemangiomatosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
350520019 | Pulmonary capillary hemangiomatosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
622204010 | Pulmonary capillary hemangiomatosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
1012841000172116 | hémangiomatose capillaire pulmonaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3386851001000110 | Hämangiomatose, kapilläre pulmonale | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
An autosomal recessive subtype of primary pulmonary hypertension which has histological characteristics of widespread fibrous intimal proliferation of septal veins and preseptal venules. There is frequent association with pulmonary capillary dilatation and proliferation and the disease can cause occult alveolar haemorrhage. | Is a | True | Pulmonary capillary haemangiomatosis | Inferred relationship | Some | |
Pulmonary hypertension due to pulmonary capillary hemangiomatosis (disorder) | Due to | True | Pulmonary capillary haemangiomatosis | Inferred relationship | Some | 2 |
Reference Sets
Description inactivation indicator reference set