Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5074053017 | Smoldering systemic mastocytosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5074054011 | Smouldering systemic mastocytosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5074055012 | Smoldering systemic mastocytosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5074064019 | SSM - smoldering systemic mastocytosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5074065018 | SSM - smouldering systemic mastocytosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5074062015 | A rare slowly progressive form of systemic mastocytosis (SM) with characteristics of gradual accumulation of neoplastic mast cells in the visceral organs. Patients typically present with splenomegaly, hypercellular marrow and in most cases urticaria pigmentosa-like skin lesions. Although the aetiology is not fully understood, an activating mutation of KIT, usually KIT D816V, is found in the mast cells of virtually all cases. This mutation probably accounts for the abnormal accumulation of mast cells in organs/tissues. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5074063013 | A rare slowly progressive form of systemic mastocytosis (SM) with characteristics of gradual accumulation of neoplastic mast cells in the visceral organs. Patients typically present with splenomegaly, hypercellular marrow and in most cases urticaria pigmentosa-like skin lesions. Although the etiology is not fully understood, an activating mutation of KIT, usually KIT D816V, is found in the mast cells of virtually all cases. This mutation probably accounts for the abnormal accumulation of mast cells in organs/tissues. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Smoldering systemic mastocytosis | Is a | Systemic mast cell disease (disorder) | false | Inferred relationship | Some | ||
| Smoldering systemic mastocytosis | Is a | Chronic disease | true | Inferred relationship | Some | ||
| Smoldering systemic mastocytosis | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
| Smoldering systemic mastocytosis | Associated morphology | Smoldering systemic mastocytosis | true | Inferred relationship | Some | 1 | |
| Smoldering systemic mastocytosis | Is a | Malignant mastocytosis | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR