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Adenosine deaminase deficiency

Diseases of the Blood and Immune Mechanism

Adenosine deaminase deficiency, often shortened to ADA deficiency, is a metabolic disorder that causes immunodeficiency. It is caused by mutations in the ADA gene and accounts for roughly ten to twenty percent of the autosomal recessive forms of severe combined immunodeficiency, once disorders related to inbreeding are excluded. According to the Wikipedia lead it can first appear in infancy, childhood, adolescence or adulthood, and the age of onset and the severity are related to some twenty nine known genotypes associated with the disorder. It occurs in fewer than one in one hundred thousand live births worldwide. This entry records what the lead states and is not medical advice.

Facts
Classification
Body System
Lymphatic or Immune System 1
ICD-10 Chapter
III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 2
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Sources
1. Adenosine deaminase deficiency (Wikipedia)
  • Lead section
    It is caused by mutations in the ADA gene
  • Lead section [body-system]
    is a metabolic disorder that causes immunodeficiency
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2. National Library of Medicine Clinical Tables: ICD-10-CM codes named Adenosine deaminase deficiency
National Library of Medicine Clinical TablesICD-10-CM list, code and name
Quote, ICD-10-CM list, code and name
"D81.30", "Adenosine deaminase deficiency, unspecified"
View the Source
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