F13A1

coagulation factor XIII A chain
OMIM: 134570
PanelMode of inheritanceDetails
2 panels
R-numbers: R90
Signed-off version 4.16
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
Factor XIIIA deficiency, OMIM:613225
R-numbers: R122
Signed-off version 1.5
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Factor XIIIA deficiency, OMIM:613225, factor XIII, A subunit, deficiency of, MONDO:0013187