Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
362175013 | Acquired C1 esterase inhibitor deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3915188019 | Acquired angioedema | en | Synonym | Active | Case insensitive | SNOMED CT core |
3915189010 | Acquired angio-oedema | en | Synonym | Active | Case insensitive | SNOMED CT core |
5034960018 | Acquired angioedema with C1Inh (C1 esterase inhibitor) deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5034961019 | Acquired angioneurotic edema with C1Inh (C1 esterase inhibitor) deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5034963016 | Acquired angioneurotic oedema with C1Inh (C1 esterase inhibitor) deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5034964010 | Acquired angioneurotic edema with C1 inhibitor deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5034967015 | Acquired angioneurotic oedema with C1 inhibitor deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
631293015 | Acquired C1 esterase inhibitor deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
5034965011 | A rare non-histaminic angioedema characterised by potentially life-threatening episodes of oedema of subcutaneous and/or mucosal tissues without urticaria, caused by excessive consumption of C1 esterase inhibitor (C1-INH) in the context of lymphoproliferative or autoimmune diseases. Patients typically present in the fourth decade of life or later and without a family history of angioedema. Clinical manifestation includes nonpitting oedema of the skin predominantly involving the face, but also the limbs or genitals, as well as abdominal pain due to involvement of the gastrointestinal mucosa and severe oedema of the upper airway and oral mucosa. Laboratory examination shows low C1-INH activity and low C3, C4, and C1q levels. Autoantibodies to C1-INH are frequently detectable. | en | Definition | Active | Case sensitive | SNOMED CT core |
5034966012 | A rare non-histaminic angioedema characterized by potentially life-threatening episodes of edema of subcutaneous and/or mucosal tissues without urticaria, caused by excessive consumption of C1 esterase inhibitor (C1-INH) in the context of lymphoproliferative or autoimmune diseases. Patients typically present in the fourth decade of life or later and without a family history of angioedema. Clinical manifestation includes nonpitting edema of the skin predominantly involving the face, but also the limbs or genitals, as well as abdominal pain due to involvement of the gastrointestinal mucosa and severe edema of the upper airway and oral mucosa. Laboratory examination shows low C1-INH activity and low C3, C4, and C1q levels. Autoantibodies to C1-INH are frequently detectable. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Acquired angioedema due to lymphoproliferative disorder | Is a | True | Acquired C1 esterase inhibitor deficiency | Inferred relationship | Some | |
Acquired angioedema due to C1 inhibitor autoantibody | Is a | True | Acquired C1 esterase inhibitor deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set