Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
350829012 | Familial pulmonary capillary haemangiomatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
350830019 | Familial pulmonary capillary hemangiomatosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
622444017 | Familial pulmonary capillary hemangiomatosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3993500012 | 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. | en | Definition | Active | Case sensitive | SNOMED CT core |
3993501011 | 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 hemorrhage. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Pulmonary hypertension due to familial pulmonary capillary haemangiomatosis | Due to | True | Familial pulmonary capillary haemangiomatosis | Inferred relationship | Some | 2 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set