Diagnosis Code D67
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.
- 286.1 - Cong factor IX disorder
- Congenital factor IX deficiency variant
- Congenital factor IX deficiency with inhibitor
- Congenital factor IX deficiency without inhibitor
- Hereditary factor IX deficiency disease
- Hereditary factor IX deficiency disease with inhibitor
- Hereditary factor IX deficiency disease without inhibitor
- Mild hereditary factor IX deficiency disease with inhibitor
- Mild hereditary factor IX deficiency disease without inhibitor
- Moderate hereditary factor IX deficiency disease with inhibitor
- Moderate hereditary factor IX deficiency disease without inhibitor
- Severe hereditary factor IX deficiency disease with inhibitor
- Severe hereditary factor IX deficiency disease without inhibitor
Index of Diseases and Injuries
References found for the code D67 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.
- Christmas disease
- Factor IX 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)
- Hemophilia B
- Plasma thromboplastin component [PTC] deficiency
Information for Patients
Also called: Christmas disease, Factor IX deficiency, Factor VIII deficiency
Hemophilia is a rare disorder in which the blood does not clot normally. It is usually inherited. Hemophilia usually occurs in males.
If you have hemophilia, you have little or no clotting factor. Clotting factor is a protein needed for normal blood clotting. Without it, you may bleed for a long time after an injury or accident. You also may bleed into your knees, ankles, and elbows. Bleeding in the joints causes pain and, if not treated, can lead to arthritis. Bleeding in the brain, a very serious complication of hemophilia, requires emergency treatment.
The main symptoms of hemophilia are excessive bleeding and easy bruising. Blood tests can tell if you have it. The main treatment is injecting the missing clotting factor into the bloodstream. You may need it on a regular basis, or just when bleeding occurs.
NIH: National Heart, Lung, and Blood Institute
- Hemophilia (Medical Encyclopedia)
- Hemophilia A (Medical Encyclopedia)
- Hemophilia B (Medical Encyclopedia)
- Partial thromboplastin time (PTT) (Medical Encyclopedia)
Hemophilia Hemophilia is a bleeding disorder that slows the blood clotting process. People with this condition experience prolonged bleeding or oozing following an injury, surgery, or having a tooth pulled. In severe cases of hemophilia, continuous bleeding occurs after minor trauma or even in the absence of injury (spontaneous bleeding). Serious complications can result from bleeding into the joints, muscles, brain, or other internal organs. Milder forms of hemophilia do not necessarily involve spontaneous bleeding, and the condition may not become apparent until abnormal bleeding occurs following surgery or a serious injury.The major types of this condition are hemophilia A (also known as classic hemophilia or factor VIII deficiency) and hemophilia B (also known as Christmas disease or factor IX deficiency). Although the two types have very similar signs and symptoms, they are caused by mutations in different genes. People with an unusual form of hemophilia B, known as hemophilia B Leyden, experience episodes of excessive bleeding in childhood but have few bleeding problems after puberty.