D68.01
BillableVon Willebrand disease, type 1
Von Willebrand disease, type 1
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Partial quantitative deficiency of von Willebrand factor
- Type 1C von Willebrand disease
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(5)
Also Known As / Clinical Terms(44)
SNOMED CT
- Hereditary von Willebrand disease type 1128106003
- von Willebrand disease type 1128106003
- Hereditary von Willebrand disease type 1B128113003
- Hereditary von Willebrand disease type IB128113003
- von Willebrand disease type IB128113003
- Hereditary von Willebrand disease type 1C128114009
- Hereditary von Willebrand disease type IC128114009
- von Willebrand disease type IC128114009
- Hereditary von Willebrand disease type 1A359700009
- Hereditary von Willebrand disease type IA359700009
- Hereditary von Willebrand disease1259242002
UMLS
- Hereditary von Willebrand disease type 1C1264039
- Hereditary von Willebrand disease type 1 (disorder)C1264039
- Type 1 von Willebrand DiseaseC1264039
- Type I von Willebrand DiseaseC1264039
- VON WILLEBRAND DISEASE, TYPE 1C1264039
- VON WILLEBRAND DISEASE, TYPE IC1264039
- VWD, TYPE 1C1264039
- VWD1C1264039
- Von Willebrand disease, type 1C1264039
- von Willebrand Disease, Type 1C1264039
- von Willebrand Disease, Type IC1264039
- von Willebrand disease type 1C1264039
- Partial quantitative deficiency of von Willebrand factorC5676304
- Type 1C von Willebrand diseaseC5676305
Clinical Terms
- von Willebrand disease type IB
- von Willebrand disease type 1
- VWD, TYPE 1
- Type 1C von Willebrand disease
- Type 1 von Willebrand Disease
- Hereditary von Willebrand disease type 1
- Hereditary von Willebrand disease type 1B
- Hereditary von Willebrand disease type 1C
- von Willebrand disease type IC
- Hereditary von Willebrand disease type IB
- Partial quantitative deficiency of von Willebrand factor
- Type I von Willebrand Disease
- von Willebrand Disease, Type I
- Hereditary von Willebrand disease type 1 (disorder)
- Hereditary von Willebrand disease type 1A
- Hereditary von Willebrand disease
- VWD1
- Hereditary von Willebrand disease type IA
- Hereditary von Willebrand disease type IC
Frequently Asked Questions
What is the ICD-10 code for von willebrand disease, type 1?
The ICD-10-CM code for von willebrand disease, type 1 is D68.01. The full clinical description is "Von Willebrand disease, type 1". D68.01 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D68.01 mean?
ICD-10-CM code D68.01 represents “Von Willebrand disease, type 1”. 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 D68.01 a billable code?
Yes, D68.01 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D68.01 in?
D68.01 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D68.01?
D68.01 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 D68.01 map to?
D68.01 maps to 5 SNOMED CT concepts: 1259242002, 128106003, 359700009, 128113003, 128114009. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D68.01?
D68.01 is linked to 3 UMLS Concept Unique Identifiers: C1264039, C5676304, C5676305. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D68.01 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like von willebrand disease, type 1 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 D68.01?
There is no direct ICD-11 mapping available for D68.01 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.