fibrinogen new orleans

Preferred Label : fibrinogen new orleans;

MeSH note : inherited abnormal fibrinogen which causes delayed cleavage of fibrinopeptide A;

Is substance : O;

Details

Origin ID

C033919;

UMLS CUI

C0615940;

Automatic exact mappings (from CISMeF team)
- fibrinogen new orleans i [SNOMED Notion]
- fibrinogen new orleans ii [SNOMED Notion]
MeSH indexing information
- coagulation protein disorders [MeSH Descriptor]
MeSH term(s) associated for indexing
- fibrinogens, abnormal [MeSH Descriptor]
Record concept(s)
- fibrinogen new orleans [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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