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

D68.4 – Acquired coagulation factor deficiency

Overview

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

Type 1 Excludes

vitamin K deficiency of newborn (P53)

Applicable To

Deficiency of coagulation factor due to liver disease
Deficiency of coagulation factor due to vitamin K deficiency

GEM Conversion to ICD-9 CM

Fs: 10000 – Acquired coagulation factor deficiency

MDC / MS-DRG Reference

COAGULATION DISORDERS

Back Reference of Diagnostic Codes

Defect, defective Q89.9
coagulation (factor) See also Deficiency, factor D68.9
acquired D68.4
due to
liver disease D68.4
vitamin K deficiency D68.4
Deficiency, deficient
AC globulin (congenital) (hereditary) D68.2
acquired D68.4
coagulation NOS D68.9
acquired (any) D68.4
due to
hyperprothrombinemia D68.4
liver disease D68.4
vitamin K deficiency D68.4
factor See also Deficiency, coagulation
multiple (congenital) D68.8
acquired D68.4
fibrin-stabilizing factor (congenital) (hereditary) D68.2
acquired D68.4
labile factor (congenital) (hereditary) D68.2
acquired D68.4
proaccelerin (congenital) (hereditary) D68.2
acquired D68.4
proconvertin factor (congenital) (hereditary) D68.2
acquired D68.4
prothrombin (congenital) (heredItary) D68.2
acquired D68.4
stable factor (congenital) (hereditary) D68.2
acquired D68.4
Fibrinopenia (hereditary) D68.2
acquired D68.4
Hemophilia (classical) (familial) (hereditary) D66
calcipriva See also Defect, coagulation D68.4
nonfamilial See also Defect, coagulation D68.4
Hyperprothrombinemia, causing coagulation factor deficiency D68.4
Hypoprothrombinemia (congenital) (hereditary) (idiopathic) D68.2
acquired D68.4

Sibling Codes

Von Willebrand's disease
Hereditary factor XI deficiency
Hereditary deficiency of other clotting factors
Hemorrhagic disorder due to circulating anticoagulants
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
D68.4 Acquired coagulation factor deficiency
Type 1 Excludes
vitamin K deficiency of newborn (P53)

Applicable to
Deficiency of coagulation factor due to liver disease
Deficiency of coagulation factor due to vitamin K deficiency