FGG

fibrinogen gamma chain
OMIM: 134850
PanelMode of inheritanceDetails
2 panels
R-numbers: R90
Signed-off version 1.2
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
202400 Afibrinogenemia, congenital, 616004 Hypodysfibrinogenemia, congenital, 616004 Dysfibrinogenemia, congenital
Green
in Thrombophilia
R-numbers: R97
Signed-off version 1.2
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
202400 Afibrinogenemia, congenital, 616004 Dysfibrinogenemia, congenital, 202400 Afibrinogenemia, congenital, 616004 Dysfibrinogenemia, congenital, 616004 Hypodysfibrinogenemia, congenital, 616004 Hypodysfibrinogenemia, congenital