D68.2 - Hereditary deficiency of other clotting factors

The ICD 10 Code for Hereditary deficiency of other clotting factors is listed as D68.2.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field	Value
Diagnosis Code:	D68.2
Description:	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) Hypoproconvertinemia Owren's disease Proaccelerin deficiency
Diagnostic Related Groups (MS-DRG v30.0)	813 - Coagulation Disorders

Chapter	Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
Block	Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
Parent	D68 - Other coagulation defects
ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD 9 Dx Code:	286.3 - Congenital deficiency of other clotting factors
ICD-10-CM Siblings (same level / similar specificity) of D68.2:
D68.0 - Von Willebrand's disease
D68.1 - Hereditary factor XI deficiency
D68.3 - Hemorrhagic disorder due to circulating anticoagulants
D68.4 - Acquired coagulation factor deficiency
D68.5 - Primary thrombophilia
D68.6 - Other thrombophilia
D68.8 - Other specified coagulation defects
D68.9 - Coagulation defect, unspecified