Congenital hypofibrinogenemia
id:
congenital-hypofibrinogenemia-316-8315735
title:
Congenital hypofibrinogenemia
text:
Congenital hypofibrinogenemia is a rare disorder in which one of the three genes responsible for producing fibrinogen, a critical blood clotting factor, is unable to make a functional fibrinogen glycoprotein because of an inherited mutation. In consequence, liver cells, the normal site of fibrinogen production, make small amounts of this critical coagulation protein, blood levels of fibrinogen are low, and individuals with the disorder may develop a coagulopathy, i.e. a diathesis or propensity t
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/Congenital_hypofibrinogenemia
date created:
date modified:
2023-08-29T18:32:49Z
main entity:
{"identifier":"Q42417401","url":"https://www.wikidata.org/entity/Q42417401"}
image:
fields total:
13
integrity:
14