fibrinogen baltimore I

Preferred Label : fibrinogen baltimore I;

MeSH note : congenital abnormal fibrinogen; polymerization defect associated with a gamma(292)Gly replaced by Val(GGC--GTC) mutation;

CISMeF synonym : fibrinogen st. gallen I;

Is substance : O;

Details

Origin ID

C066651;

UMLS CUI

C0314579;

Currated CISMeF NLP mapping
- Fibrinogen Baltimore I (substance) [SNOMED CT concept]
- fibrinogen baltimore i [SNOMED Notion]
MeSH indexing information
- coagulation protein disorders [MeSH Descriptor]
MeSH term(s) associated for indexing
- fibrinogens, abnormal [MeSH Descriptor]
Record concept(s)
- fibrinogen Baltimore I [MeSH concept]
- fibrinogen st. gallen I [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- Fibrinogen Baltimore I (substance) [SNOMED CT concept]
- fibrinogen baltimore i [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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