Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
351503014 | Combined phagocytic defect | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
622932011 | Combined phagocytic defect (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4996941000241115 | déficit phagocytaire combiné | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
anémie hémolytique auto-immune avec érythrophagocytose (Fc portion de l'auto-anticorps) | Is a | False | Combined phagocytic defect | Inferred relationship | Some | |
Chédiak-Higashi syndrome | Is a | True | Combined phagocytic defect | Inferred relationship | Some | |
A rare genetic primary immunodeficiency characterized by profound circulating monocytopenia, B- and NK-cell lymphopenia and severe dendritic cell decrease, which manifests clinically with disseminated mycobacterial and viral infections, as well as opportunistic fungal and parasitic infections and frequent pulmonary alveolar proteinosis. Predisposition to developing myeloid neoplasms is associated. | Is a | True | Combined phagocytic defect | Inferred relationship | Some | |
Haemophagocytic lymphohistiocytosis | Is a | True | Combined phagocytic defect | Inferred relationship | Some |
This concept is not in any reference sets