ICD 10 CM Codes

D68.2 Hereditary deficiency of other clotting factors
Billable Code  is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
GEMS
ICD-10-CM D68.2 converts approximately to:ICD-9-CM
2015 ICD-9-CM 286.3 Congenital deficiency of other clotting factors
ICD-10-CM D68.2is grouped within Diagnostic Related Group(s) (MS-DRG v30.0)
813 COAGULATION DISORDERS
Alternate Description
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
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.D68.2.'
Absence (of) (organ or part) (complete or partial); fibrinogen (congenital)
Afibrinogenemia; congenital
Defect, defective; coagulation (factor); hereditary NEC
Defect, defective; fibrin polymerization
Defect, defective; Hageman (factor)
Deficiency, deficient; accelerator globulin (Ac G) (blood)
Deficiency, deficient; AC globulin (congenital) (hereditary)
Deficiency, deficient; activating factor (blood)
Deficiency, deficient; autoprothrombin; I
Deficiency, deficient; autoprothrombin; C
Deficiency, deficient; clotting factor NEC (hereditary)
Deficiency, deficient; coagulation NOS; clotting factor NEC
Deficiency, deficient; contact factor
Deficiency, deficient; factor; Hageman
Deficiency, deficient; factor; I (congenital) (hereditary)
Deficiency, deficient; factor; II (congenital) (hereditary)
Deficiency, deficient; factor; V (congenital) (hereditary)
Deficiency, deficient; factor; VII (congenital) (hereditary)
Deficiency, deficient; factor; X (congenital) (hereditary)
Deficiency, deficient; factor; XII (congenital) (hereditary)
Deficiency, deficient; factor; XIII (congenital) (hereditary)
Deficiency, deficient; fibrin-stabilizing factor (congenital) (hereditary)
Deficiency, deficient; fibrinase
Deficiency, deficient; fibrinogen (congenital) (hereditary)
Deficiency, deficient; glass factor
Deficiency, deficient; Hageman factor
Deficiency, deficient; labile factor (congenital) (hereditary)
Deficiency, deficient; Laki-Lorand factor
Deficiency, deficient; proaccelerin (congenital) (hereditary)
Deficiency, deficient; proconvertin factor (congenital) (hereditary)
Deficiency, deficient; prothrombin (congenital) (heredItary)
Deficiency, deficient; Prower factor
Deficiency, deficient; SPCA (factor VII)
Deficiency, deficient; stable factor (congenital) (hereditary)
Deficiency, deficient; Stuart-Prower (factor X)
Deficiency, deficient; thrombokinase
Disease, diseased; Hageman (congenital factor XII deficiency)
Disease, diseased; Stuart-Prower (congenital factor X deficiency)
Disease, diseased; Stuart's (congenital factor X deficiency)
Dysfibrinogenemia (congenital)
Fibrinogenopenia; congenital
Fibrinopenia (hereditary)
Hageman's factor defect, deficiency or disease
Hypofibrinogenemia; congenital (hereditary)
Hypoproconvertinemia, congenital (hereditary)
Hypoprothrombinemia (congenital) (hereditary) (idiopathic)
Owren's disease or syndrome (parahemophilia)
Parahemophilia
Stuart deficiency disease (factor X)
Stuart-Prower factor deficiency (factor X)
Syndrome; Owren's