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ICD-10-CM Codes D50-D89 D65-D69 D68 D68.2

ICD-10-CM Diagnosis Code D68.2

Effective Date: 10/01/2015 To 09/30/2025

Hereditary deficiency of other clotting factors

CMS-HCC-V24	CMS-HCC-V28	RxHCC	Age	Gender	Maternity	Acute or Chronic	MCC
48	112	--	--	--	--	Chronic	No

Applicable To for D68.2:

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

Back-references to D68.2

Absence(of) (organ or part) (complete or partial)

fibrinogen(congenital) D68.2

Afibrinogenemia see also Defect, coagulation D68.8

congenital D68.2

Defect, defective Q89.9

Hageman(factor) D68.2
coagulation(factor) see also Deficiency, factor D68.9
- hereditary NEC D68.2
fibrin polymerization D68.2

Deficiency, deficient

AC globulin(congenital) (hereditary) D68.2
Hageman factor D68.2
Laki-Lorand factor D68.2
Prower factor D68.2
SPCA(factor VII) D68.2
Stuart-Prower(factor X) D68.2
accelerator globulin(Ac G) (blood) D68.2
activating factor(blood) D68.2
autoprothrombin
- C D68.2
- I D68.2
clotting factor NEC(hereditary) see also Deficiency, factor D68.2
coagulation NOS D68.9
- clotting factor NEC see also Deficiency, factor D68.2
contact factor D68.2
factor see also Deficiency, coagulation
- Hageman D68.2
- I(congenital) (hereditary) D68.2
- II(congenital) (hereditary) D68.2
- V(congenital) (hereditary) D68.2
- VII(congenital) (hereditary) D68.2
- X(congenital) (hereditary) D68.2
- XII(congenital) (hereditary) D68.2
- XIII(congenital) (hereditary) D68.2
fibrin-stabilizing factor(congenital) (hereditary) D68.2
fibrinase D68.2
fibrinogen(congenital) (hereditary) D68.2
glass factor D68.2
labile factor(congenital) (hereditary) D68.2
proaccelerin(congenital) (hereditary) D68.2
proconvertin factor(congenital) (hereditary) D68.2
prothrombin(congenital) (heredItary) D68.2
stable factor(congenital) (hereditary) D68.2
thrombokinase D68.2

Disease, diseased see also Syndrome

Hageman(congenital factor XII deficiency) D68.2
Stuart's(congenital factor X deficiency) D68.2
Stuart-Prower(congenital factor X deficiency) D68.2

Dysfibrinogenemia(congenital) D68.2

Fibrinogenopenia D68.8

congenital D68.2

Fibrinopenia(hereditary) D68.2

Hageman's factor defect, deficiency or disease D68.2

Hypofibrinogenemia D68.8

congenital(hereditary) D68.2

Hypoproconvertinemia, congenital(hereditary) D68.2

Hypoprothrombinemia(congenital) (hereditary) (idiopathic) D68.2

Owren's disease or syndrome(parahemophilia) D68.2

Parahemophilia see also Defect, coagulation D68.2

Stuart deficiency disease(factor X) D68.2

Stuart-Prower factor deficiency(factor X) D68.2

Syndrome see also Disease

Owren's D68.2

Related Medications for D68.2

factor ix, coagulation factor vii, factor viia, coagulation factor viii

Chapter, Section and Diagnosis Prefix for D68.2

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Coagulation defects, purpura and other hemorrhagic conditions

Other coagulation defects