Inherited bleeding disorders
Gene: FGAEnsemblGeneIds (GRCh38): ENSG00000171560
EnsemblGeneIds (GRCh37): ENSG00000171560
OMIM: 134820, Gene2Phenotype
FGA is in 5 panels
2 reviews
Louise Daugherty (Genomics England Curator)
Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Fibrinogen deficiency
BRIDGE consortium (NIHRBR-RD)
Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Fibrinogen deficiency
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- BOTH monoallelic and biallelic, autosomal or pseudoautosomal
- Sources
-
- Other
- Radboud University Medical Center, Nijmegen
- Expert Review Green
- BRIDGE Study Tier 1 Gene
- Phenotypes
-
- Fibrinogen deficiency
- Hypodysfibrinogenemia,congenital,616004
- Dysfibrinogenemia,congenital,616004
- thrombosis
- Fibrinogen Dusart
- dysfibrinogenemia associated with recurrent thrombosis
- thrombophilia
- prolonged thrombin clotting
- Fibrinogen Caracas II
- OMIM
- 134820
- Clinvar variants
- Variants in FGA
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
panel promoted to version 1
Louise Daugherty (Genomics England Curator)Revised 19 December 2016
Added New Source
Ellen McDonagh (Genomics England Curator)FGA was added to Inherited bleeding disorderspanel. Source: Radboud University Medical Center, Nijmegen FGA was added to Inherited bleeding disorderspanel. Source: Other
Added New Source
Louise Daugherty (Genomics England Curator)FGA was added to Inherited bleeding disorderspanel. Source: Expert Review Green
Added New Source
Ellen McDonagh (Genomics England Curator)FGA was added to Inherited bleeding disorderspanel. Sources: BRIDGE Study Tier 1 Gene
Created
Ellen McDonagh (Genomics England Curator)FGA was created by ellenmcdonagh