hereditary angioedema type III

Preferred Label : hereditary angioedema type III;

UMLS semantic type : T046 - Pathologic Function;

Origin ID

M0529317;

UMLS CUI

C1857728;

Automatic exact mappings (from CISMeF team)
- Hereditary angioedema type III [MedDRA LLT]
Currated CISMeF NLP mapping
- Angioedema, hereditary, 3 [OMIM Phenotype]
- F12-related hereditary angioedema with normal C1Inh [ORDO Disease]
- Hereditary angioedema type III [ICD-11 More detail]
- hereditary angioedema type III [Disease (Nov.)]
Related record
- hereditary angioedema type III [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Angioedema, hereditary, 3 [OMIM Phenotype]
- F12-related hereditary angioedema with normal C1Inh [ORDO Disease]
- Hereditary angioedema type III [MedDRA LLT]
- hereditary angioedema type III [Disease (Nov.)]