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Afibrinogenemia

Disease Afferent Pupillary DefectAflatoxins

Afibrinogenemia
Overview
Congenital afibrinogenemia is a rare, inherited blood disorder in which the blood does not clot normally.

 


Afibrinogenemia, Congenital
National Organization for Rare Disorders, Inc.
Synonyms ...

Congenital afibrinogenemia is a rare, inherited blood disorder in which the blood does not clot normally. It occurs when there is a lack (deficiency) of a protein called fibrinogen, which is needed for the blood to clot.
Causes ...

Afibrinogenemia
Related Terms
Congenital Afibrogenemia
Congenital Blood Disorder
Congenital Deficiency of Other Clotting Factors
Fibrinogen Deficiency ...

Afibrinogenemia, Congenital Causes, Symptoms And Treatment And Related Disorders ...

Afibrinogenemia, Congenital
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AGA
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Age-Related Macular Degeneration, Laser Photocoagulation for ...

Congenital afibrinogenemia
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Disseminated intravascular coagulation (DIC) ...

Congenital afibrinogenemia
Congenital antithrombin III deficiency
Congenital cataract
Congenital cytomegalovirus
Congenital heart disease
Congenital nephrogenic diabetes insipidus
Congenital nephrotic syndrome ...

Congenital Afibrinogenemia ... blood in urine
Congenital aplastic anemia ... blood in urine
Congenital disorder of glycosylation type 1A ... proteinuria
Congenital disorder of glycosylation type 2H ... bladder incontinence ...

See also: Symptom, Bleeding, Congenital afibrinogenemia, Deficiency, Surgery

Disease Afferent Pupillary DefectAflatoxins

 
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