Genomics England
GMS Panels
Panels
Genes and Entities

FGA

fibrinogen alpha chain
OMIM: 134820
PanelMode of inheritanceDetails
3 panels
Green
in Bleeding and platelet disorders
R-numbers: R90
Signed-off version 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
202400 Afibrinogenemia, congenital, 616004 Hypodysfibrinogenemia, congenital, 105200 Amyloidosis, familial visceral, 616004 Dysfibrinogenemia, congenital
Green
in Hereditary systemic amyloidosis
R-numbers: R204
Signed-off version 1.18
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Amyloidosis, familial visceral, OMIM:105200
Green
in Thrombophilia with a likely monogenic cause
R-numbers: R97
Signed-off version 2.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
202400 Afibrinogenemia, congenital, 105200 Amyloidosis, familial visceral, 616004 Dysfibrinogenemia, congenital, 616004 Hypodysfibrinogenemia, congenital