ICD-10-CM Codes
D50-D89
D65-D69
D68-
2023 ICD-10-CM Diagnosis Code D68.022

2023 ICD-10-CM Diagnosis Code D68.022

Von Willebrand disease, type 2M

2023 - New Code

Billable/Specific Code

D68.022 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
ICD-10-CM D68.022 is a new 2023 ICD-10-CM code that became effective on October 1, 2022.
This is the American ICD-10-CM version of D68.022 - other international versions of ICD-10 D68.022 may differ.

Applicable To

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

The following code(s) above D68.022 contain annotation back-references

Annotation Back-References

In this context, annotation back-references refer to codes that contain:

Applicable To annotations, or
Code Also annotations, or
Code First annotations, or
Excludes1 annotations, or
Excludes2 annotations, or
Includes annotations, or
Note annotations, or
Use Additional annotations

that may be applicable to D68.022:

D50-D89
2023 ICD-10-CM Range D50-D89
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Type 2 Excludes
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
D68
ICD-10-CM Diagnosis Code D68
Other coagulation defects
Type 1 Excludes
- abnormal coagulation profile NOS (R79.1)
Type 2 Excludes
- coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
- coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)
Other coagulation defects
D68.0
ICD-10-CM Diagnosis Code D68.0
Von Willebrand disease
Type 1 Excludes
- capillary fragility (hereditary) (D69.8)
- factor VIII deficiency NOS (D66)
- factor VIII deficiency with functional defect (D66)
Von Willebrand disease
D68.02
ICD-10-CM Diagnosis Code D68.02
Von Willebrand disease, type 2
Applicable To
- Qualitative defects of von Willebrand factor
Von Willebrand disease, type 2

ICD-10-CM D68.022 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):

813 Coagulation disorders

Code History

2023 (effective 10/1/2022): New code

Diagnosis Index entries containing back-references to D68.022:

Defect, defective Q89.9
ICD-10-CM Diagnosis Code Q89.9
Congenital malformation, unspecified
Applicable To
Congenital anomaly NOS
Congenital deformity NOS
- qualitative, of von Willebrand factor
  - with
    - defective platelet adhesion with a normal size distribution of von Willebrand factor multimers D68.022 - see also Disease, von Willebrand
Disease, diseased - see also Syndrome
- von Willebrand (-Jürgens) (angiohemophilia) D68.00
  ICD-10-CM Diagnosis Code D68.00
  Von Willebrand disease, unspecified
  2023 - New Code Billable/Specific Code
  - type 2 D68.029
    ICD-10-CM Diagnosis Code D68.029
    Von Willebrand disease, type 2, unspecified
    2023 - New Code Billable/Specific Code
    Applicable To
    Qualitative defect in von Willebrand factor function, with no further subtyping
    - type 2M D68.022

ICD-10-CM Codes Adjacent To D68.022

D65 Disseminated intravascular coagulation [defibrination syndrome]

D66 Hereditary factor VIII deficiency

D67 Hereditary factor IX deficiency

D68 Other coagulation defects

D68.0 Von Willebrand disease

D68.00 …… unspecified

D68.01 …… type 1

D68.02 Von Willebrand disease, type 2

D68.020 ……A

D68.021 ……B

D68.022 ……M

D68.023 ……N

D68.029 …… unspecified

D68.03 …… type 3

D68.04 Acquired von Willebrand disease

D68.09 Other von Willebrand disease

D68.1 Hereditary factor XI deficiency

D68.2 Hereditary deficiency of other clotting factors

D68.3 Hemorrhagic disorder due to circulating anticoagulants

D68.31 Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

D68.311 Acquired hemophilia

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

2023 ICD-10-CM Diagnosis Code D68.022

Von Willebrand disease, type 2M

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

Other coagulation defects

Von Willebrand disease

Von Willebrand disease, type 2

Congenital malformation, unspecified

Von Willebrand disease, unspecified

Von Willebrand disease, type 2, unspecified