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ICD-10-CM Code D68.0
Von Willebrand's disease

Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
| ICD-10 from 2011 - 2016

D68.0 is a billable ICD code used to specify a diagnosis of von Willebrand's disease. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

The ICD code D680 is used to code Von Willebrand disease

Von Willebrand disease (vWD) (/ˌfʌnˈvɪlᵻbrɑːnt/) is the most common hereditary coagulation abnormality described in humans, although it can also be acquired as a result of other medical conditions. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. It is known to affect humans and dogs (notably Doberman Pinschers), and rarely swine, cattle, horses, and cats. There are three forms of vWD: hereditary, acquired, and pseudo or platelet type. There are three types of hereditary vWD: vWD type 1, vWD type 2, and vWD type 3. Within the three inherited types of vWD there are various subtypes. Platelet type vWD is also an inherited condition.

Specialty: Hematology
MeSH Code: D014842
ICD 9 Code: 286.4
Source: Wikipedia

Coding Notes for D68.0 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
Factor VIII deficiency with vascular defect
Vascular hemophilia
Code Type-1 Excludes:
Type-1 Excludes
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."
Capillary fragility (hereditary) - instead, use code D69.8
Factor VIII deficiency NOS - instead, use Code D66
Factor VIII deficiency with functional defect - instead, use Code D66

MS-DRG Mapping

  • DRG Group #813 - Coagulation disorders.

ICD-10-CM Alphabetical Index References for 'D68.0 - Von Willebrand's disease'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D68.0. Click on any term below to browse the alphabetical index.

Willebrand(-Jürgens) thrombopathy (D68.0)
Von Willebrand(-Jurgens)(-Minot) disease or syndrome (D68.0)
Pseudohemophilia(Bernuth's) (hereditary) (type B) (D68.0)
Minot-von Willebrand-Jurgens disease or syndrome(angiohemophilia) (D68.0)
Angiohemophilia(A) (B) (D68.0)


Von Willebrand's disease (exact match)

This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 286.4 was previously used, D68.0 is the appropriate modern ICD10 code.

Parent Code: D68 - Other coagulation defects

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/D680