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82966003: Hereditary angioedema (disorder)

Status: current, 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
137607018 Hereditary angioneurotic edema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
137609015 Hereditary Quincke's edema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
137610013 Hereditary angioedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
201052011 Hereditary Quincke's oedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
505363019 Hereditary angioneurotic oedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1216996012 HANE - Hereditary angioneurotic oedema en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1216997015 HAE - Hereditary angio-oedema en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1216998013 Hereditary angio-oedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1218486018 HANE - Hereditary angioneurotic edema en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1218487010 HAE - Hereditary angioedema en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009695016 Hereditary angioedema (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3943505015 Inherited form of angioedema caused by decreased levels or function of C1 inhibitor or other mechanisms including mutations of the genes encoding coagulation factor XII, angiopoietin-1, plasminogen and as yet undefined factors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
137607018 Hereditary angioneurotic edema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
137607018 Hereditary angioneurotic edema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
137608011 C-1 esterase inhibitor deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
137609015 Hereditary Quincke's edema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
137610013 Hereditary angioedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
137610013 Hereditary angioedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
201052011 Hereditary Quincke's oedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
505363019 Hereditary angioneurotic oedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
505363019 Hereditary angioneurotic oedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
824499012 Hereditary angioneurotic edema (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216996012 HANE - Hereditary angioneurotic oedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216996012 HANE - Hereditary angioneurotic oedema en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1216997015 HAE - Hereditary angio-oedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216997015 HAE - Hereditary angio-oedema en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1216998013 Hereditary angio-oedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216998013 Hereditary angio-oedema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1218486018 HANE - Hereditary angioneurotic edema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1218486018 HANE - Hereditary angioneurotic edema en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1218487010 HAE - Hereditary angioedema en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1218487010 HAE - Hereditary angioedema en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1234766019 C1 esterase inhibitor deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1234766019 C1 esterase inhibitor deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009695016 Hereditary angioedema (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009695016 Hereditary angioedema (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3009876013 Inherited form of angioedema caused by decreased levels or function of C1 inhibitor or other mechanisms leading to increased levels of bradykinin en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3943505015 Inherited form of angioedema caused by decreased levels or function of C1 inhibitor or other mechanisms including mutations of the genes encoding coagulation factor XII, angiopoietin-1, plasminogen and as yet undefined factors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3432831001000119 Angioödem, hereditäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
870281000172119 angio-oedème héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
968011000172116 angio-oedème bradykinique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50009651000188113 oedème angioneurotique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50009671000188118 angio-oedème non histaminique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50009681000188115 angio-oedème familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
870281000172119 angio-oedème héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
968011000172116 angio-oedème bradykinique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50009651000188113 oedème angioneurotique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50009671000188118 angio-oedème non histaminique héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
50009681000188115 angio-oedème familial fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3432831001000119 Angioödem, hereditäres de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary angio-oedema Is a Hereditary disorder of the integument (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Is a Angioedema true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Is a Complement regulatory factor defect false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Is a Hereditary disorder of immune system false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Finding site Structure of immune system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary angio-oedema Associated morphology Urticaria false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary angio-oedema Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Is a Angioedema due to disorder of kinin metabolism false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angio-oedema Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary angio-oedema Associated morphology Angioedema (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary angio-oedema Is a Hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary C1 esterase inhibitor deficiency - deficient factor Is a False Hereditary angio-oedema Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Is a False Hereditary angio-oedema Inferred relationship Existential restriction modifier (core metadata concept)
Acquired C1 esterase inhibitor deficiency Is a False Hereditary angio-oedema Inferred relationship Existential restriction modifier (core metadata concept)
ACE inhibitor-aggravated angioedema-urticaria (disorder) Is a False Hereditary angio-oedema Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary angioneurotic oedema with normal C1 esterase inhibitor activity Is a True Hereditary angio-oedema Inferred relationship Existential restriction modifier (core metadata concept)
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. Is a True Hereditary angio-oedema Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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