|
D68.0 |
Von Willebrand's disease |
| Billable Code | is a billable ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. |
| GEMS |
| ICD-10-CM D68.0 converts approximately to:ICD-9-CM |
| 2015 ICD-9-CM 286.4 Von Willebrand's disease |
| ICD-10-CM D68.0is grouped within Diagnostic Related Group(s) (MS-DRG v30.0) |
| 813 COAGULATION DISORDERS
|
| Type 1 Excludes |
| capillary fragility (hereditary) (D69.8) |
| factor VIII deficiency NOS (D66) |
| factor VIII deficiency with functional defect (D66) |
| Alternate Description |
| Angiohemophilia |
| Factor VIII deficiency with vascular defect |
| Vascular hemophilia |
| ICD-10-CM Index Entry |
| ICD-10-CM Index entries containing back-references to ICD-10-CM '.D68.0.' |
| Angiohemophilia (A) (B) |
| Defect, defective; platelets, qualitative; constitutional |
| Deficiency, deficient; factor; VIII (congenital) (functional) (hereditary) (with functional defect); with vascular defect |
| Deficiency, deficient; platelet NEC; constitutional |
| Disease, diseased; Minot-von Willebrand-Jürgens (angiohemophilia) |
| Disease, diseased; von Willebrand (-J ürgens) (angiohemophilia) |
| Hemophilia (classical) (familial) (hereditary); vascular |
| Minot-von Willebrand-Jurgens disease or syndrome (angiohemophilia) |
| Pseudohemophilia (Bernuth's) (hereditary) (type B) |
| Syndrome; von Willebrand (-J ürgen) |
| Syndrome; Willebrand (-J ürgens) |
| Thrombopathy (Bernard-Soulier); constitutional |
| Thrombopathy (Bernard-Soulier); Willebrand-Jurgens |
| Von Willebrand (-Jurgens)(-Minot) disease or syndrome |
| Willebrand (-J ürgens) thrombopathy |
