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Term:
Parent Terms Term With Siblings Child Terms
Acquired Hypoprothrombinemia 
Congenital Prothrombin Deficiency  
n extremely rare autosomal recessive bleeding disorder characterized by low levels of circulating prothrombin. There are 2 main types: type I deficiency, known as true prothrombin deficiency or 'hypoprothrombinemia,' is defined as plasma levels of prothrombin being less than 10% of normal with a concomitant decrease in activity. Type II deficiency, known as 'dysprothrombinemia,' is characterized by normal or low-normal synthesis of a dysfunctional protein.

Synonyms
Exact Synonyms: HEREDITARY FACTOR II DEFICIENCY DISEASE ;   HYPOPROTHROMBINEMIA ;   PROTHROMBIN DEFICIENCY, CONGENITAL
Related Synonyms: DYSPROTHROMBINEMIA ;   PROLONGED PROTHROMBIN TIME
Primary IDs: OMIM:613679

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