fibrinogen tottori II

Preferred Label : fibrinogen tottori II;

MeSH note : congenital hypofibrinogenemia is caused by a nonsense mutation in the fibrinogen Bbeta chain gene mutation (TAT sequence for Bbeta 41Tyr to TAG sequence for a translation termination signal);

Is substance : O;

Details

Origin ID

C489711;

UMLS CUI

C1506267;

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

Keyword's position in hierarchy(ies) :

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