234620006: Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)

SNOMED CT Concept\Clinical finding\...

\Edema\Disorder characterized by edema\Angioedema and/or urticaria\Angioedema\...

\Angioedema due to disorder of kinin metabolism\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor

\Hereditary angioedema\Hereditary angioedema with C1 esterase inhibitor deficiency\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
\Disease\Genetic disease\Hereditary disease\Hereditary angioedema\Hereditary angioedema with C1 esterase inhibitor deficiency\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
\Disease\Disorder of immune function\Hereditary disorder of immune system\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
\Disease\Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Disorder of complement\Complement deficiency disease\Complement regulatory factor defect\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
\Disease\Disorder of body system\Disorder of immune structure\Complement regulatory factor defect\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
\Disease\Disorder characterized by edema\Angioedema and/or urticaria\Angioedema\Angioedema due to disorder of kinin metabolism\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
\Disease\Disorder characterized by edema\Angioedema and/or urticaria\Angioedema\Hereditary angioedema\Hereditary angioedema with C1 esterase inhibitor deficiency\Hereditary C1 esterase inhibitor deficiency - dysfunctional factor

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

351542014 Hereditary angioneurotic edema - type 2 en Synonym Active Entire term case insensitive SNOMED CT core module

351543016 Hereditary angio-oedema - type 2 en Synonym Active Entire term case insensitive SNOMED CT core module

351544010 Hereditary angioneurotic oedema - type 2 en Synonym Active Entire term case insensitive SNOMED CT core module

351545011 C1 esterase inhibitor deficiency - type 2 en Synonym Active Entire term case sensitive SNOMED CT core module

351546012 Hereditary C1 esterase inactivity en Synonym Active Only initial character case insensitive SNOMED CT core module

351547015 Hereditary C1 esterase inhibitor deficiency - dysfunctional factor en Synonym Active Only initial character case insensitive SNOMED CT core module

622965015 Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

2161483018 Hereditary angioedema - type 2 en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Is a	Hereditary angioedema	false	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Associated morphology	Urticaria	false	Inferred relationship	Existential restriction modifier	1
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Finding site	Structure of immune system	true	Inferred relationship	Existential restriction modifier	2
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Associated morphology	Inflammation	false	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Is a	Angioedema due to disorder of C1 esterase inhibitor	false	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Pathological process	Abnormal immune process	false	Inferred relationship	Existential restriction modifier	3
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Pathological process	Abnormal immune process	true	Inferred relationship	Existential restriction modifier	2
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Is a	Hereditary disorder of immune system	true	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Is a	Complement regulatory factor defect	true	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Associated morphology	Angioedema	true	Inferred relationship	Existential restriction modifier	1
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Is a	Angioedema due to disorder of kinin metabolism	true	Inferred relationship	Existential restriction modifier
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Causative agent	Kallidin I	true	Inferred relationship	Existential restriction modifier	1
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	Is a	Hereditary angioedema with C1 esterase inhibitor deficiency	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
351542014	Hereditary angioneurotic edema - type 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
351543016	Hereditary angio-oedema - type 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
351544010	Hereditary angioneurotic oedema - type 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
351545011	C1 esterase inhibitor deficiency - type 2	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
351546012	Hereditary C1 esterase inactivity	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
351547015	Hereditary C1 esterase inhibitor deficiency - dysfunctional factor	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
622965015	Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
2161483018	Hereditary angioedema - type 2	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module