D68.020
BillableVon Willebrand disease, type 2A
Von Willebrand disease, type 2A
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight 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) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-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
Related Codes(4)
Also Known As / Clinical Terms(24)
SNOMED CT
UMLS
- Hereditary von Willebrand disease type 2AC1282968
- Hereditary von Willebrand disease type 2A (disorder)C1282968
- Type 2A von Willebrand DiseaseC1282968
- Type IIA von Willebrand DiseaseC1282968
- VON WILLEBRAND DISEASE, TYPE 2AC1282968
- VWD2AC1282968
- Von Willebrand disease, type 2AC1282968
- von Willebrand Disease, Type 2AC1282968
- von Willebrand Disease, Type IIAC1282968
- Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimersC5676307
Clinical Terms
- von Willebrand disease type 2
- Type IIA von Willebrand Disease
- Hereditary von Willebrand disease
- Qualitative defects of von Willebrand factor with decreased platelet adhesion and selective deficiency of high-molecular-weight multimers
- Type 2A von Willebrand Disease
- von Willebrand Disease, Type IIA
- VWD2A
- Hereditary von Willebrand disease type 2
- Hereditary von Willebrand disease type 2A (disorder)
- Hereditary von Willebrand disease type 2A
Frequently Asked Questions
What is the ICD-10 code for von willebrand disease, type 2a?
The ICD-10-CM code for von willebrand disease, type 2a is D68.020. The full clinical description is "Von Willebrand disease, type 2A". D68.020 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D68.020 mean?
ICD-10-CM code D68.020 represents “Von Willebrand disease, type 2A”. 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 D68.020 a billable code?
Yes, D68.020 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D68.020 in?
D68.020 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D68.020?
D68.020 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 D68.020 map to?
D68.020 maps to 3 SNOMED CT concepts: 1259242002, 128107007, 359711001. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D68.020?
D68.020 is linked to 2 UMLS Concept Unique Identifiers: C1282968, C5676307. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D68.020 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like von willebrand disease, type 2a affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D68.020?
There is no direct ICD-11 mapping available for D68.020 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.