D68.2ICD-10-CM 2027 · Billable
Hereditary deficiency of other clotting factors
Sibling codes
D68.0– Von Willebrand diseaseD68.1– Hereditary factor XI deficiencyD68.3– Hemorrhagic disorder due to circulating anticoagulantsD68.4– Acquired coagulation factor deficiencyD68.5– Primary thrombophiliaD68.6– Other thrombophiliaD68.8– Other specified coagulation defectsD68.9– Coagulation defect, unspecified
Inclusion terms
- 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
Inherited from D68: Other coagulation defects
Excludes1
- abnormal coagulation profile NOS (
R79.1)
Excludes2
Part of: D68: Other coagulation defects