FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

846575004: Angioedema (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3914361011 Angioedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3914362016 Angioedema (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3914540015 Angio-oedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Angioedema Is a Edema true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Angioedema Associated morphology True Angioedema Inferred relationship Some 1
Food-induced angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Drug-aggravated angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Episodic angioedema with eosinophilia (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Angioedema due to disorder of kinin metabolism Associated morphology True Angioedema Inferred relationship Some 1
Vibratory angioedema (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Venom-induced angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Physical angioedema (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Cholinergic angioedema (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Angioedema of tongue (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Angioedema of eyelid (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Angioedema of lip (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Penicillin-induced angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Idiopathic angioedema (disorder) Associated morphology True Angioedema Inferred relationship Some 1
ACE inhibitor-aggravated angioedema Associated morphology True Angioedema Inferred relationship Some 1
Aspirin-induced angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Autoimmune angioedema (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Chemical-aggravated angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Respiratory angioedema Associated morphology True Angioedema Inferred relationship Some 1
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. Associated morphology True Angioedema Inferred relationship Some 1
Acquired angio-oedema due to the presence of neutralising antibodies against C1 inhibitor. Associated morphology True Angioedema Inferred relationship Some 1
Azo-dye-induced angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Sodium benzoate-induced angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Latex-induced angioedema-urticaria Associated morphology False Angioedema Inferred relationship Some 2
Allergic angioedema (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Allergic angioedema due to bite and/or sting (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Allergic angioedema due to ingested food (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Angioedema caused by angiotensin-converting-enzyme inhibitor (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Intestinal angioedema caused by angiotensin-converting enzyme inhibitor (disorder) Associated morphology True Angioedema Inferred relationship Some 1
NSAID-induced angioedema-urticaria Associated morphology True Angioedema Inferred relationship Some 2
ACE inhibitor-aggravated angioedema Associated morphology True Angioedema Inferred relationship Some 2
Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain. Associated morphology True Angioedema Inferred relationship Some 1
Hereditary C1 esterase inhibitor deficiency - deficient factor Associated morphology True Angioedema Inferred relationship Some 1
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Associated morphology True Angioedema Inferred relationship Some 1
Hereditary angioedema without abnormal C1 inhibitor levels or function. One type has been found mostly in females in which symptoms may be triggered by pregnancy or estrogen-containing oral contraceptives. Mechanisms include mutations of the genes encoding coagulation factor XII, angiopoietin-1, plasminogen and as yet undefined factors. Associated morphology True Angioedema Inferred relationship Some 1
Angioedema caused by angiotensin-converting-enzyme inhibitor (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Intestinal angioedema caused by angiotensin-converting enzyme inhibitor (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Acquired angioedema due to activation of the classical complement pathway related to an underlying lymphoreticular disorder particularly lymphoma or monoclonal gammopathy of unknown significance (MGUS) Associated morphology True Angioedema Inferred relationship Some 1
Drug-induced angioedema-urticaria (disorder) Associated morphology True Angioedema Inferred relationship Some 2
Hevea brasiliensis latex protein-induced angioedema-urticaria Associated morphology True Angioedema Inferred relationship Some 2
Angioedema of gingiva due to deficiency of C1 esterase inhibitor Associated morphology True Angioedema Inferred relationship Some 1
A rare hereditary angioedema characterized by potentially life-threatening episodes of subcutaneous and/or submucosal edema without urticaria, associated with C1 esterase inhibitor (C1-INH) deficiency. Hereditary angioedema (HAE) type 1 is caused by quantitative, HAE type 2 by qualitative defects of C1-INH. The two subtypes are clinically indistinguishable. Patients may present at any age (but most commonly in childhood) with recurrent attacks of nonpitting edema of the skin, severe abdominal symptoms such as pain and swelling, and/or respiratory distress due to upper respiratory airways involvement. Genital, bladder, muscle, or joint swelling may occur in some cases. Associated morphology True Angioedema Inferred relationship Some 1
Acquired angioedema type II (disorder) Associated morphology True Angioedema Inferred relationship Some 1
Acquired angioedema type I (disorder) Associated morphology True Angioedema Inferred relationship Some 1

This concept is not in any reference sets

Back to Start