D68.022
BillableVon Willebrand disease, type 2M
Von Willebrand disease, type 2M
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimers
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- 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)
- 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)
Also Known As / Clinical Terms
SNOMED CT
UMLS
- Qualitative defects of von Willebrand factor with defective platelet adhesion with a normal size distribution of von Willebrand factor multimersC5676311
- Type 2M von Willebrand DiseaseC1282974
- Type IIM von Willebrand DiseaseC1282974
- VON WILLEBRAND DISEASE, TYPE 2MC1282974
- VWD2MC1282974
- Von Willebrand disease, type 2MC1282974
- von Willebrand Disease, Type 2MC1282974
- von Willebrand Disease, Type IIMC1282974
Frequently Asked Questions
What is the ICD-10 code for von willebrand disease, type 2m?
The ICD-10-CM code for von willebrand disease, type 2m is D68.022. The full clinical description is "Von Willebrand disease, type 2M". D68.022 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D68.022 mean?
ICD-10-CM code D68.022 represents "Von Willebrand disease, type 2M". It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D68.022 a billable code?
Yes, D68.022 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D68.022 in?
D68.022 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D68.022?
D68.022 has Excludes1 notes indicating codes that cannot be used together with it, including: abnormal coagulation profile NOS (R79.1); capillary fragility (hereditary) (D69.8); factor VIII deficiency NOS (D66); and 1 more.
What SNOMED CT codes does D68.022 map to?
D68.022 maps to 3 SNOMED CT concepts: 1259242002, 128107007, 359725000. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D68.022?
D68.022 is linked to 2 UMLS Concept Unique Identifiers: C5676311, C1282974. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.