kininogen deficiency, total

Preferred Label : kininogen deficiency, total;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0565865;

UMLS CUI

C1856719;

Automatic exact mappings (from CISMeF team)
- High molecular weight kininogen deficiency [OMIM Phenotype]
Currated CISMeF NLP mapping
- Total kininogen deficiency [HPO term]
Related record
- flaujeac factor deficiency [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Total kininogen deficiency [HPO term]