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dysfibrinogenemia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
FGG
FGB
FGA
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
Fibrinogen, alpha/beta/gamma chain, coiled coil domain
fibrinogen complex
REACTOME_COMMON_PATHWAY
REACTOME_GRB2_SOS_PROVIDES_LINKAGE_TO_MAPK_SIGNALING_FOR_INTERGRINS_
REACTOME_P130CAS_LINKAGE_TO_MAPK_SIGNALING_FOR_INTEGRINS
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Most Correlated Studies
OMIM - Blood coagulation disorders
OMIM - Congenital disorder
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Literature
Most Relevant Literature
The FGG c.952G>A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral inf…
Management of congenital dysfibrinogenemia in pregnancy: A challenging patient case.
How I treat dysfibrinogenemia.
Pedigree Analysis and Diagnosis of Congenital Dysfibrinogenemia: A Case Report].
Dysfibrinogenemia-Potential Impact of Genotype on Thrombosis or Bleeding.
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Most Relevant Clinical Trials
Genomics of Fibrin Clot Structure in Patients With Constitutional Dysfibrinogenemia
Pregnancy and Fibrinogen Disorders
Ex Vivo Laboratory Assays Application for Therapy Tailoring in Patients With Severe Bleeding Disorde…
Safety and Efficacy of Fibryga in Congenital Fibrinogen Deficiency
Transfusion of Red Blood Cells, Tranexamic Acid and Fibrinogen Concentrate for Severe Trauma Hemorrh…
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