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

D68.0 – Von Willebrand's disease

Overview

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

Type 1 Excludes

capillary fragility (hereditary) (D69.8)
factor VIII deficiency NOS (D66)
factor VIII deficiency with functional defect (D66)

Applicable To

Angiohemophilia
Factor VIII deficiency with vascular defect
Vascular hemophilia

GEM Conversion to ICD-9 CM

Fs: 00000 – Von Willebrand's disease

MDC / MS-DRG Reference

COAGULATION DISORDERS

Back Reference of Diagnostic Codes

Angiohemophilia (A) (B) D68.0
Defect, defective Q89.9
platelets, qualitative D69.1
constitutional D68.0
Deficiency, deficient
factor See also Deficiency, coagulation
VIII (congenital) (functional) (hereditary) (with functional defect) D66
with vascular defect D68.0
platelet NEC D69.1
constitutional D68.0
Disease, diseased See also Syndrome
Minot-von Willebrand-Jürgens (angiohemophilia) D68.0
von Willebrand (-Jürgens) (angiohemophilia) D68.0
Hemophilia (classical) (familial) (hereditary) D66
vascular D68.0
Minot-von Willebrand-Jurgens disease or syndrome (angiohemophilia) D68.0
Pseudohemophilia (Bernuth's) (hereditary) (type B) D68.0
Syndrome See also Disease
von Willebrand (-Jürgen) D68.0
Willebrand (-Jürgens) D68.0
Thrombopathy (Bernard-Soulier) D69.1
constitutional D68.0
Willebrand-Jurgens D68.0
Von Willebrand disease or syndrome (-Jurgens)(-Minot) D68.0
Willebrand thrombopathy (-Jürgens) D68.0

Sibling Codes

Hereditary factor XI deficiency
Hereditary deficiency of other clotting factors
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
D68.0 Von Willebrand's disease
Type 1 Excludes
capillary fragility (hereditary) (D69.8)
factor VIII deficiency NOS (D66)
factor VIII deficiency with functional defect (D66)

Applicable to
Angiohemophilia
Factor VIII deficiency with vascular defect
Vascular hemophilia