Dysfibrinogenemia, familial (medical condition)

A rare familial disorder characterized by abnormal fibrinogen. There are various types of this order and they can vary in severity from asymptomatic to causing abnormal bleeding and blood clotting. Examples of subtypes includes Amsterdam, Detroit and Wiesbaden dysfibrinogenemia. See also Dysfibrinogenemia, 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.