fibrinogen vlissingen

Preferred Label : fibrinogen vlissingen;

MeSH note : congenitally abnormal fibrinogen with a 6-base deletion in the gamma-chain gene, causing defective calcium binding & impaired fibrin polymerization;

Is substance : O;

Details

Origin ID

C069866;

UMLS CUI

C0646822;

MeSH term(s) associated for indexing
- fibrinogens, abnormal [MeSH Descriptor]
Record concept(s)
- fibrinogen vlissingen [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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