Diagnosis Code D68.0
Information for Medical Professionals
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
- 286.4 - Von willebrand's disease
- Acquired coagulation factor inhibitor disorder
- Acquired von Willebrand's disease
- Congenital von Willebrand's disease
- Congenital von Willebrand's disease type I
- Congenital von Willebrand's disease type II
- Congenital von Willebrand's disease type III
- Drug-induced coagulation inhibitor disorder
- Glycoprotein Ib defect
- Hereditary von Willebrand disease type 2A
- Hereditary von Willebrand disease type 2B
- Hereditary von Willebrand disease type 2M
- Hereditary von Willebrand disease type IA
- Platelet membrane defect
- Platelet type von Willebrand's disease
- von Willebrand disease type 1
- von Willebrand disease type 2
- von Willebrand disease type 2A
- von Willebrand disease type 2B
- von Willebrand disease type 2M
- von Willebrand disease type 2N
- von Willebrand disease type 3
- von Willebrand disease type IA
- von Willebrand disease type IB
- von Willebrand disease type IC
- von Willebrand disease, type 1^a^
- von Willebrand disease, type IIA
- von Willebrand disease, type IIB
- von Willebrand disease, type IIC
- von Willebrand disease, type IID
- von Willebrand disease, type IIE
- von Willebrand disease, type IIF
- von Willebrand disease, type IIG
- von Willebrand disease, type IIH
- von Willebrand disorder
- von Willebrand factor inhibitor disorder
Index of Diseases and Injuries
References found for the code D68.0 in the Index of Diseases and Injuries:
- Inclusion Terms: Inclusion terms
List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of “other specified” codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- Factor VIII deficiency WITH "With"
The word “with” should be interpreted to mean “associated with” or “due to” when it appears in a code title, the Alphabetic Index, or an instructional note in the Tabular List. The word “with” in the Alphabetic Index is sequenced immediately following the main term, not in alphabetical order. vascular defect
- Vascular hemophilia
- Type 1 Excludes Notes: Type 1 Excludes Notes
A type 1 Excludes note is a pure excludes note. It means “NOT CODED HERE!” An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- capillary fragility (hereditary) (D69.8)
- factor VIII deficiency NOS (D66)
- factor VIII deficiency WITH "With"
The word “with” should be interpreted to mean “associated with” or “due to” when it appears in a code title, the Alphabetic Index, or an instructional note in the Tabular List. The word “with” in the Alphabetic Index is sequenced immediately following the main term, not in alphabetical order. functional defect (D66)
Information for Patients
Also called: Thrombocyte disorders
Platelets are little pieces of blood cells. Platelets help wounds heal and prevent bleeding by forming blood clots. Your bone marrow makes platelets. Problems can result from having too few or too many platelets, or from platelets that do not work properly.
If your blood has a low number of platelets, it is called thrombocytopenia. This can put you at risk for mild to serious bleeding. If your blood has too many platelets, you may have a higher risk of blood clots. With other platelet disorders, the platelets do not work as they should. For example, in von Willebrand Disease, the platelets cannot stick together or cannot attach to blood vessel walls. This can cause excessive bleeding.
Treatment of platelet disorders depends on the cause.
NIH: National Heart, Lung, and Blood Institute
- Bleeding time
- Congenital platelet function defects
- Glanzmann disease
- Idiopathic thrombocytopenic purpura (ITP)
- Partial thromboplastin time (PTT)
- Platelet aggregation test
- Primary thrombocythemia
- Thromobocytopenia - drug-induced
Von Willebrand disease Von Willebrand disease is a bleeding disorder that slows the blood clotting process, causing prolonged bleeding after an injury. People with this condition often experience easy bruising, long-lasting nosebleeds, and excessive bleeding or oozing following an injury, surgery, or dental work. Mild forms of von Willebrand disease may become apparent only when abnormal bleeding occurs following surgery or a serious injury. Women with this condition typically have heavy or prolonged bleeding during menstruation (menorrhagia), and some may also experience reproductive tract bleeding during pregnancy and childbirth. In severe cases of von Willebrand disease, heavy bleeding occurs after minor trauma or even in the absence of injury (spontaneous bleeding). Symptoms of von Willebrand disease may change over time. Increased age, pregnancy, exercise, and stress may cause bleeding symptoms to become less frequent.Von Willebrand disease is divided into three types, with type 2 being further divided into four subtypes. Type 1 is the mildest and most common of the three types, accounting for 75 percent of affected individuals. Type 3 is the most severe and rarest form of the condition. The four subtypes of type 2 von Willebrand disease are intermediate in severity. Another form of the disorder, acquired von Willebrand syndrome, is not caused by inherited gene mutations. Acquired von Willebrand syndrome is typically seen along with other disorders, such as diseases that affect bone marrow or immune cell function. This rare form of the condition is characterized by abnormal bleeding into the skin and other soft tissues, usually beginning in adulthood.