ICD-10-CM Book 2026 Edition
Chapters ICD-10-CM Book Table of Content /
chapter 3 D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism /
D65-D69 Coagulation defects, purpura and other hemorrhagic conditions /
D68 Other coagulation defects
Billable ICD-10-CM Code D68.2
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D68.2
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Hereditary deficiency of other clotting factors
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| 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) | |||
| Hypoproconvertinemia | |||
| Owren's disease | |||
| Proaccelerin deficiency |