Thrombomodulin anomalies, familial (medical condition)

A defect in a protein involved with anticoagulation which results in an increased risk of developing blood clots which can result in death. See also Thrombomodulin anomalies, familial

Chemwatch
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.