ICD-10-CM Current in FY 2027

D68.022

Von Willebrand disease, type 2M

Hierarchy

Where D68.022 sits in the official hierarchy. Each level is the code it is classified under.

Reproduced verbatim from the FY 2027 ICD-10-CM files. Notes labelled as inherited are declared on a parent code and apply here too.

Inclusion Terms

Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers

Excludes1

capillary fragility (hereditary) ( D69.8 )

Inherited from D68.0 — Von Willebrand disease

Excludes1

abnormal coagulation profile NOS ( R79.1 )

Inherited from D68 — Other coagulation defects

Excludes1

factor VIII deficiency NOS ( D66 )

Inherited from D68.0 — Von Willebrand disease

Excludes1

factor VIII deficiency with functional defect ( D66 )

Inherited from D68.0 — Von Willebrand disease

Excludes2

coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1 )

Inherited from D68 — Other coagulation defects

Excludes2

coagulation defects complicating pregnancy, childbirth and the puerperium ( O45.0 , O46.0 , O67.0 , O72.3 )

Inherited from D68 — Other coagulation defects

How D68.022 appears in each release imported from the official files, newest first.

Code information on this page is derived from the FY 2027 ICD-10-CM files published by CDC NCHS and CMS.

MedCodeSearch is an independent reference service and is not affiliated with CMS, CDC, or the U.S. government.

Search ICD-10-CM, ICD-10-PCS and HCPCS Level II by code or description.