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ICD-10-CM Codes Browse (Tabular) Diagnostic External Drug Neoplasm

D68.2 – Hereditary deficiency of other clotting factors

Overview

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

Applicable To

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

GEM Conversion to ICD-9 CM

Fs: 00000 – Congenital deficiency of other clotting factors

MDC / MS-DRG Reference

COAGULATION DISORDERS

Back Reference of Diagnostic Codes

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
coagulation (factor) See also Deficiency, factor D68.9
hereditary NEC D68.2
fibrin polymerization D68.2
Hageman (factor) D68.2
Deficiency, deficient
accelerator globulin (Ac G) (blood) D68.2
AC globulin (congenital) (hereditary) D68.2
activating factor (blood) D68.2
autoprothrombin
I D68.2
C 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
Hageman factor D68.2
labile factor (congenital) (hereditary) D68.2
Laki-Lorand factor D68.2
proaccelerin (congenital) (hereditary) D68.2
proconvertin factor (congenital) (hereditary) D68.2
prothrombin (congenital) (heredItary) D68.2
Prower factor D68.2
SPCA (factor VII) D68.2
stable factor (congenital) (hereditary) D68.2
Stuart-Prower (factor X) D68.2
thrombokinase D68.2
Disease, diseased See also Syndrome
Hageman (congenital factor XII deficiency) D68.2
Stuart-Prower (congenital factor X deficiency) D68.2
Stuart's (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

Sibling Codes

Von Willebrand's disease
Hereditary factor XI deficiency
Hemorrhagic disorder due to circulating anticoagulants
Acquired coagulation factor deficiency
Primary thrombophilia
Other thrombophilia
Other specified coagulation defects
Coagulation defect, unspecified

Parent Sibling Codes

Acquired pure red cell aplasia [erythroblastopenia]
Other aplastic anemias and other bone marrow failure syndromes
Acute posthemorrhagic anemia
Anemia in chronic diseases classified elsewhere
Other anemias
Disseminated intravascular coagulation [defibrination syndrome]
Hereditary factor VIII deficiency
Hereditary factor IX deficiency
Other coagulation defects
Purpura and other hemorrhagic conditions

View in Tabular

Code Title
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
D65-D69 Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
D68 Other coagulation defects
D68.2 Hereditary deficiency of other clotting factors
Applicable to
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