Valid for Submission
D71 is a billable diagnosis code used to specify a medical diagnosis of functional disorders of polymorphonuclear neutrophils. The code D71 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.
The ICD-10-CM code D71 might also be used to specify conditions or terms like 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, etc.
Tabular List of Diseases and Injuries
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code D71:
Inclusion TermsInclusion Terms
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
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code D71 are found in the index:
- - Disease, diseased - See Also: Syndrome;
- - Disorder (of) - See Also: Disease;
- - Dysphagocytosis, congenital - D71
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- 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
- Functional disorders of polymorphonuclear neutrophils
- Granulomatous disorder
- Heritable disorder of neutrophil function
- Hypercalcemia due to granulomatous disease
- Hypoparathyroidism due to granulomatous disease
- Interstitial lung disease due to granulomatous disease
- Neutrophil lactoferrin deficiency
Diagnostic Related Groups - MS-DRG Mapping
Convert D71 to ICD-9 Code
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.