TBXA2R

thromboxane A2 receptor
OMIM: 188070, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber TBXA2R in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Amber
Phenotypes
  • {Bleeding disorder, platelet-type, 13, susceptibility to}, MIM# 614009