Diagnosis Code D71
Information for Medical Professionals
The diagnosis code D71 is grouped in the following Diagnostic Related Group(s) (MS-DRG V35.0)
- 808 - MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH
- 809 - MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH
- 810 - MAJOR HEMATOLOGICAL AND IMMUNOLOGICAL DIAGNOSES EXCEPT SICKLE CELL CRISIS AND COAGULATION DISORDERS WITH
Convert to ICD-9 General Equivalence Map
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.
- 288.1 - Function dis neutrophils
- Chronic granulomatous disease
- Chronic granulomatous disease, type I
- Chronic granulomatous disease, type IA
- Chronic granulomatous disease, type II
- Chronic granulomatous disease, type IIA
- Chronic granulomatous disease, type III
- Chronic granulomatous disease, type IV
- Chronic granulomatous disease, type IVA
- Disorder characterized by granuloma formation
- Functional disorders of polymorphonuclear neutrophils
- Heritable disorder of neutrophil function
- Hypercalcemia due to granulomatous disease
- Neutrophil lactoferrin deficiency
Index of Diseases and Injuries
References found for the code D71 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.
- Cell membrane receptor complex [CR3] defect
- Chronic (childhood) granulomatous disease
- Congenital dysphagocytosis
- Progressive septic granulomatosis
Information for Patients
Also called: Hematologic diseases
Your blood is living tissue made up of liquid and solids. The liquid part, called plasma, is made of water, salts and protein. Over half of your blood is plasma. The solid part of your blood contains red blood cells, white blood cells and platelets.
Blood disorders affect one or more parts of the blood and prevent your blood from doing its job. They can be acute or chronic. Many blood disorders are inherited. Other causes include other diseases, side effects of medicines, and a lack of certain nutrients in your diet.
Types of blood disorders include
- Platelet disorders, excessive clotting, and bleeding problems, which affect how your blood clots
- Anemia, which happens when your blood does not carry enough oxygen to the rest of your body
- Cancers of the blood, such as leukemia and myeloma
- Eosinophilic disorders, which are problems with one type of white blood cell.
- Blood differential test (Medical Encyclopedia)
- Blood smear (Medical Encyclopedia)
- CBC (Medical Encyclopedia)
- Hematocrit (Medical Encyclopedia)
- Hemoglobin (Medical Encyclopedia)
- Low white blood cell count and cancer (Medical Encyclopedia)
- RBC count (Medical Encyclopedia)
- RBC indices (Medical Encyclopedia)
- WBC count (Medical Encyclopedia)
Chronic granulomatous disease Chronic granulomatous disease is a disorder that causes the immune system to malfunction, resulting in a form of immunodeficiency. Immunodeficiencies are conditions in which the immune system is not able to protect the body from foreign invaders such as bacteria and fungi. Individuals with chronic granulomatous disease may have recurrent bacterial and fungal infections. People with this condition may also have areas of inflammation (granulomas) in various tissues that can result in damage to those tissues. The features of chronic granulomatous disease usually first appear in childhood, although some individuals do not show symptoms until later in life.People with chronic granulomatous disease typically have at least one serious bacterial or fungal infection every 3 to 4 years. The lungs are the most frequent area of infection; pneumonia is a common feature of this condition. Individuals with chronic granulomatous disease may develop a type of fungal pneumonia, called mulch pneumonitis, which causes fever and shortness of breath after exposure to decaying organic materials such as mulch, hay, or dead leaves. Exposure to these organic materials and the numerous fungi involved in their decomposition causes people with chronic granulomatous disease to develop fungal infections in their lungs. Other common areas of infection in people with chronic granulomatous disease include the skin, liver, and lymph nodes.Inflammation can occur in many different areas of the body in people with chronic granulomatous disease. Most commonly, granulomas occur in the gastrointestinal tract and the genitourinary tract. In many cases the intestinal wall is inflamed, causing a form of inflammatory bowel disease that varies in severity but can lead to stomach pain, diarrhea, bloody stool, nausea, and vomiting. Other common areas of inflammation in people with chronic granulomatous disease include the stomach, colon, and rectum, as well as the mouth, throat, and skin. Additionally, granulomas within the gastrointestinal tract can lead to tissue breakdown and pus production (abscesses). Inflammation in the stomach can prevent food from passing through to the intestines (gastric outlet obstruction), leading to an inability to digest food. These digestive problems cause vomiting after eating and weight loss. In the genitourinary tract, inflammation can occur in the kidneys and bladder. Inflammation of the lymph nodes (lymphadenitis) and bone marrow (osteomyelitis), which both produce immune cells, can lead to further impairment of the immune system.Rarely, people with chronic granulomatous disease develop autoimmune disorders, which occur when the immune system malfunctions and attacks the body's own tissues and organs.Repeated episodes of infection and inflammation reduce the life expectancy of individuals with chronic granulomatous disease; however, with treatment, most affected individuals live into mid- to late adulthood.