TBXA2R

thromboxane A2 receptor
OMIM: 188070
PanelMode of inheritanceDetails
1 panel
R-numbers: R90
Signed-off version 3.0
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
{Bleeding disorder, platelet-type, 13, susceptibility to}, OMIM:614009