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Diseases » ADA Deficiency » Summary

What is ADA Deficiency?

What is ADA Deficiency?

  • ADA Deficiency: Adenosine deaminase deficiency is a condition which is inherited that results severe combined immunodeficiency disease.
  • ADA Deficiency: An autosomal recessive deficiency of the purine salvage enzyme adenosine deaminase which results in Severe Combined Immunodeficiency Disease (SCID). The most common form of SCID, accounting for about 50% of autosomal recessive cases. The first disease for which gene therapy was applied.
    Source - Diseases Database

ADA Deficiency: Introduction

Types of ADA Deficiency:

Broader types of ADA Deficiency:

How serious is ADA Deficiency?

Complications of ADA Deficiency: see complications of ADA Deficiency

What causes ADA Deficiency?

Causes of ADA Deficiency: see causes of ADA Deficiency

What are the symptoms of ADA Deficiency?

Symptoms of ADA Deficiency: see symptoms of ADA Deficiency

Complications of ADA Deficiency: see complications of ADA Deficiency

Can anyone else get ADA Deficiency?

More information: see contagiousness of ADA Deficiency
Inheritance: see inheritance of ADA Deficiency

ADA Deficiency: Testing

Misdiagnosis: see misdiagnosis and ADA Deficiency.

How is it treated?

Doctors and Medical Specialists for ADA Deficiency: Medical Geneticist ; see also doctors and medical specialists for ADA Deficiency.
Treatments for ADA Deficiency: see treatments for ADA Deficiency
Research for ADA Deficiency: see research for ADA Deficiency

Name and Aliases of ADA Deficiency

Main name of condition: ADA Deficiency

Other names or spellings for ADA Deficiency:

Adenosine deaminase deficiency Source - Diseases Database

ADA Deficiency: Related Conditions

Research the causes of these diseases that are similar to, or related to, ADA Deficiency:


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