hereditary angioedema type II

Preferred Label : hereditary angioedema type II;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Origin ID

M0529320;

UMLS CUI

C1862892;

Automatic exact mappings (from CISMeF team)
- Angioedema, hereditary, 1 [OMIM Phenotype]
- Hereditary angioedema type II [MedDRA LLT]
Currated CISMeF NLP mapping
- Hereditary angioedema type 2 [ORDO Disease]
- Hereditary angioedema type II [ICD-11 More detail]
- hereditary angioedema type II [Disease (Nov.)]
Related record
- hereditary angioedema types I and II [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary angioedema type 2 [ORDO Disease]
- Hereditary angioedema type II [MedDRA LLT]
- hereditary angioedema type II [Disease (Nov.)]