Congenital afibrinogenemia: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
m Bot: Automated text replacement (-{{SIB}} + & -{{EH}} + & -{{EJ}} + & -{{Editor Help}} + & -{{Editor Join}} +) |
||
| Line 6: | Line 6: | ||
{{SI}} | {{SI}} | ||
'''Congenital afibrinogenemia''' is a rare inherited blood disorder in which the [[blood]] does not clot normally due to a lack of or a malfunction involving [[fibrinogen]], a [[protein]] necessary for [[coagulation]]. | '''Congenital afibrinogenemia''' is a rare inherited blood disorder in which the [[blood]] does not clot normally due to a lack of or a malfunction involving [[fibrinogen]], a [[protein]] necessary for [[coagulation]]. | ||
| Line 13: | Line 13: | ||
* {{OMIM|202400}} | * {{OMIM|202400}} | ||
[[Category:Congenital disorders]] | [[Category:Congenital disorders]] | ||
Revision as of 00:09, 9 August 2012
Template:DiseaseDisorder infobox
Congenital afibrinogenemia is a rare inherited blood disorder in which the blood does not clot normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation.
External links