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) 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
- 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
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.
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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.