TBXA2R

thromboxane A2 receptor
OMIM: 188070, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber TBXA2R in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.43

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

Amber TBXA2R in Mendeliome


Version 1.1891

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