kininogen deficiency, high molecular weight and low molecular weight

Preferred Label : kininogen deficiency, high molecular weight and low molecular weight;

Origin ID

C567116;

UMLS CUI

C2673570;

Automatic exact mappings (from CISMeF team)
- High molecular weight kininogen deficiency [OMIM Phenotype]
MeSH term(s) associated for indexing
- blood protein disorders [MeSH Descriptor]
- kininogens [MeSH Descriptor]
Record concept(s)
- kininogen deficiency, high molecular weight and low molecular weight [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]