Hereditary angioedema type II

Preferred Label : Hereditary angioedema type II;

ICD-11 definition : Hereditary angioedema associated with gene mutations resulting in functionally defective C1 inhibitor.;

ICD-11 synonym : C1-INH - [C1 esterase inhibitor] deficiency; C1-INH deficiency; HAE-II - [Hereditary angioedema type II]; Hereditary angioneurotic oedema type 2; C1 esterase inhibitor [C1-INH] qualitative deficiency;

ICD-11 acronym : HAE-II;

Details

Origin ID

2078615244;

Automatic exact mappings (from CISMeF team)
- Angioedema, hereditary, 1 [OMIM Phenotype]
- Hereditary angioedema type II [MedDRA LLT]
- Product containing C1 esterase inhibitor (product) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Hereditary angioedema type 2 [ORDO Disease]
- hereditary angioedema type II [MeSH concept]
- hereditary angioedema type II [Disease (Nov.)]
See also inter- (CISMeF)
- Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder) [SNOMED CT concept]
Validated automatic mappings to NTBT
- Defects in the complement system [ICD-10 Sub-category]
- hereditary angioedema types I and II [MeSH Descriptor]

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