Valid for Submission
D82.0 is a billable diagnosis code used to specify a medical diagnosis of wiskott-aldrich syndrome. The code D82.0 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 D82.0 might also be used to specify conditions or terms like dense body defect, immunodeficiency associated with multiple organ system abnormalities, immunodeficiency with major anomalies, wiskott-aldrich autosomal dominant variant syndrome or wiskott-aldrich syndrome.
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 D82.0:
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.
- Immunodeficiency with thrombocytopenia and eczema
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 D82.0 are found in the index:
- - Deficiency, deficient
- - Syndrome - See Also: Disease;
- - Aldrich (-Wiskott) - D82.0
- - eczema-thrombocytopenia - D82.0
- - familial eczema-thrombocytopenia (Wiskott-Aldrich) - D82.0
- - Wiskott-Aldrich - D82.0
- - Wiskott-Aldrich syndrome - D82.0
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Dense body defect
- Immunodeficiency associated with multiple organ system abnormalities
- Immunodeficiency with major anomalies
- Wiskott-Aldrich autosomal dominant variant syndrome
- Wiskott-Aldrich syndrome
- WISKOTT ALDRICH SYNDROME-. a rare x linked immunodeficiency syndrome characterized by eczema; lymphopenia; and recurrent pyogenic infection. it is seen exclusively in young boys. typically immunoglobulin m levels are low and immunoglobulin a and immunoglobulin e levels are elevated. lymphoreticular malignancies are common.
- WISKOTT ALDRICH SYNDROME PROTEIN FAMILY-. a family of microfilament proteins whose name derives from the fact that mutations in members of this protein family have been associated with wiskott aldrich syndrome. they are involved in actin polymerization and contain a polyproline rich region that binds to profilin and a verprolin homology domain that binds g actin.
- WISKOTT ALDRICH SYNDROME PROTEIN-. wasp protein is mutated in wiskott aldrich syndrome and is expressed primarily in hematopoietic cells. it is the founding member of the wasp protein family and interacts with cdc42 protein to help regulate actin polymerization.
- WISKOTT ALDRICH SYNDROME PROTEIN NEURONAL-. a member of the wiskott aldrich syndrome protein family that is found at high levels in nerve cells. it interacts with grb2 adaptor protein and with cdc42 protein.
Diagnostic Related Groups - MS-DRG Mapping
Convert D82.0 to ICD-9 Code
Information for Patients
Immune System and Disorders
Your immune system is a complex network of cells, tissues, and organs that work together to defend against germs. It helps your body to recognize these "foreign" invaders. Then its job is to keep them out, or if it can't, to find and destroy them.
If your immune system cannot do its job, the results can be serious. Disorders of the immune system include
- Allergy and asthma - immune responses to substances that are usually not harmful
- Immune deficiency diseases - disorders in which the immune system is missing one or more of its parts
- Autoimmune diseases - diseases causing your immune system to attack your own body's cells and tissues by mistake
NIH: National Institute of Allergy and Infectious Diseases
- Agammaglobulinemia (Medical Encyclopedia)
- Aging changes in immunity (Medical Encyclopedia)
- Chronic granulomatous disease (Medical Encyclopedia)
- Graft-versus-host disease (Medical Encyclopedia)
- Histiocytosis (Medical Encyclopedia)
- Hyperimmunoglobulin E syndrome (Medical Encyclopedia)
- Immune response (Medical Encyclopedia)
- Immunodeficiency disorders (Medical Encyclopedia)
- Selective deficiency of IgA (Medical Encyclopedia)
[Learn More in MedlinePlus]
Wiskott-Aldrich syndrome Wiskott-Aldrich syndrome is characterized by abnormal immune system function (immune deficiency), eczema (an inflammatory skin disorder characterized by abnormal patches of red, irritated skin), and a reduced ability to form blood clots. This condition primarily affects males.Individuals with Wiskott-Aldrich syndrome have microthrombocytopenia, which is a decrease in the number and size of blood cells involved in clotting (platelets). This platelet abnormality, which is typically present from birth, can lead to easy bruising, bloody diarrhea, or episodes of prolonged bleeding following nose bleeds or minor trauma. Microthrombocytopenia can also lead to small areas of bleeding just under the surface of the skin, resulting in purplish spots called purpura, or variably sized rashes made up of tiny red spots called petechiae. In some cases, particularly if a bleeding episode occurs within the brain, prolonged bleeding can be life-threatening.Wiskott-Aldrich syndrome is also characterized by abnormal or nonfunctional immune system cells known as white blood cells. Changes in white blood cells lead to an increased risk of several immune and inflammatory disorders in people with Wiskott-Aldrich syndrome. These immune problems vary in severity and include an increased susceptibility to infection from bacteria, viruses, and fungi. People with Wiskott-Aldrich syndrome are at greater risk of developing autoimmune disorders, such as rheumatoid arthritis, vasculitis, or hemolytic anemia. These disorder occur when the immune system malfunctions and attacks the body's own tissues and organs. The chance of developing certain types of cancer, such as cancer of the immune system cells (lymphoma), is also increased in people with Wiskott-Aldrich syndrome.Wiskott-Aldrich syndrome is often considered to be part of a disease spectrum with two other disorders: X-linked thrombocytopenia and severe congenital neutropenia. These conditions have overlapping signs and symptoms and the same genetic cause.
[Learn More in MedlinePlus]