ICD-10-CM Code for Hereditary deficiency of other clotting factors D68.2

ICD-10 code D68.2 for Hereditary deficiency of other clotting factors is a medical classification as listed by WHO under the range - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism .

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Hereditary deficiency of other clotting factors
AC globulin deficiency
Congenital afibrinogenemia
Deficiency of factor I [fibrinogen]
Deficiency of factor II [prothrombin]
Deficiency of factor V [labile]
Deficiency of factor VII [stable]
Deficiency of factor X [Stuart-Prower]
Deficiency of factor XII [Hageman]
Deficiency of factor XIII [fibrin stabilizing]
Dysfibrinogenemia (congenital)
Owren's disease
Proaccelerin deficiency


Excludes1: abnormal coagulation profile NOS (R79.1)

Excludes2: coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)

Get crucial instructions for accurate ICD-10-CM D68.2 coding with all applicable Excludes 1 and Excludes 2 notes from the section level conveniently shown with each code.
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