angioedemas, hereditary

Preferred Label : angioedemas, hereditary;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0502559;

UMLS CUI

C0019243;

Automatic exact mappings (from CISMeF team)
- Angioedema, hereditary, 1 [OMIM Phenotype]
- serpin family G member 1 [ORDO Gene]
Currated CISMeF NLP mapping
- Hereditary Angioedema [NCIt concept]
- Hereditary angioedema [ICD-11 Sub-sub category]
- Hereditary angioedema [HPO term]
- Hereditary angioedema [MedDRA Preferred Term]
- Hereditary angioedema [ORDO Disease]
- Hereditary angioedema (disorder) [SNOMED CT concept]
- hereditary angioedema [DO Concept]
- hereditary angioedema [Disease (Nov.)]
- hereditary angioedema [Blood Transfusion thesaurus concept]
- hereditary angioneurotic edema [SNOMED Notion]
- hereditary angioneurotic edema [TUV Concept]
- hereditary angioneurotic edema [TUV Term]
Related record
- angioedemas, hereditary [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- C1 esterase inhibitor deficiency [MedDRA LLT]
- Hereditary Angioedema [NCIt concept]
- Hereditary angioedema [HPO term]
- Hereditary angioedema [ORDO Disease]
- Hereditary angioedema [MedDRA Preferred Term]
- Hereditary angioedema [ICD-11 Sub-sub category]
- Hereditary angioedema (disorder) [SNOMED CT concept]
- Hereditary angioedema C1 inhibitor deficiency [MedDRA LLT]
- hereditary angioedema [DO Concept]
- hereditary angioedema [Disease (Nov.)]
- hereditary angioneurotic edema [TUV Concept]
- hereditary angioneurotic edema [TUV Term]
- hereditary angioneurotic edema [SNOMED Notion]