Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2023. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5159702014 | Monoclonal MCAD (mast cell activation disorder) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5159703016 | Monoclonal mast cell activation syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5159704010 | Monoclonal mast cell activation syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5159705011 | A rare haematologic disease characterised by symptoms of mast cell activation in the absence of cutaneous findings, as well as absence of diagnostic criteria of systemic mastocytosis with tryptase levels of less than 20 mg/ml and normal to low burden of mast cells. Bone marrow biopsy reveals the presence of monoclonal mast cells carrying the KIT D816V mutation and/or expressing CD25. Symptoms include recurrent episodes of flushing, headache, hypotension, abdominal cramping, nausea, diarrhoea, cardiac arrhythmia, bronchoconstriction and bleeding diathesis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5159706012 | A rare hematologic disease characterized by symptoms of mast cell activation in the absence of cutaneous findings, as well as absence of diagnostic criteria of systemic mastocytosis with tryptase levels of less than 20 mg/ml and normal to low burden of mast cells. Bone marrow biopsy reveals the presence of monoclonal mast cells carrying the KIT D816V mutation and/or expressing CD25. Symptoms include recurrent episodes of flushing, headache, hypotension, abdominal cramping, nausea, diarrhea, cardiac arrhythmia, bronchoconstriction and bleeding diathesis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Monoclonal mast cell activation syndrome (disorder) | Is a | Monoclonal gammopathy (clinical) | false | Inferred relationship | Some | ||
| Monoclonal mast cell activation syndrome (disorder) | Is a | Mast cell activation syndrome (disorder) | true | Inferred relationship | Some | ||
| Monoclonal mast cell activation syndrome (disorder) | Finding site | Mast cell | true | Inferred relationship | Some | 3 | |
| Monoclonal mast cell activation syndrome (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 4 | |
| Monoclonal mast cell activation syndrome (disorder) | Interprets | Serum globulin measurement | false | Inferred relationship | Some | 1 | |
| Monoclonal mast cell activation syndrome (disorder) | Has interpretation | Above reference range | false | Inferred relationship | Some | 1 | |
| Monoclonal mast cell activation syndrome (disorder) | Interprets | Immunoglobulin measurement | false | Inferred relationship | Some | 2 | |
| Monoclonal mast cell activation syndrome (disorder) | Has interpretation | Above reference range | false | Inferred relationship | Some | 2 | |
| Monoclonal mast cell activation syndrome (disorder) | Interprets | Paraprotein measurement | false | Inferred relationship | Some | 5 | |
| Monoclonal mast cell activation syndrome (disorder) | Has interpretation | Present | false | Inferred relationship | Some | 5 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR