FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
Disease: Hypodysfibrinogenemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		0.440 GeneticVariation disease BEFREE Fibrinogen Columbus II: A novel c.1075G>T mutation in the FGG gene causing hypodysfibrinogenemia and thrombosis in an adolescent male. 31131962 2019
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		0.440 GeneticVariation disease BEFREE Direct sequencing analyses were performed on FGA, FGB, and FGG genes to confirm hypodysfibrinogenemia and on the protein C gene to confirm protein C deficiency. 30632992 2019
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		0.440 GeneticVariation disease BEFREE We found a novel hypodysfibrinogenemia designated Tsukuba I caused by compound heterozygous nucleotide deletions with FGG c.1129+62_65 del AATA and FGG c.1299+4 del A on different alleles. 27837696 2016
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		0.440 GeneticVariation disease BEFREE A novel fibrinogen γ chain frameshift deletion (c.637delT) in a patient with hypodysfibrinogenemia associated with thrombosis. 26540127 2015
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		0.440 Biomarker disease GENOMICS_ENGLAND
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		0.440 CausalMutation disease CLINVAR