TBXA2R

thromboxane A2 receptor
OMIM: 188070
PanelMode of inheritanceDetails
1 panel
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
614009.BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO, BDPLT13, 614009 BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO