Severe combined immunodeficiency due to adenosine deaminase deficiency [Supplementary Concept]
Inherited ADA deficiency resulting in immunodeficiency. It accounts for 15 % of SCID cases in infancy. Partial ADA deficiency may occur in some immunocompetent patients, who show decreased enzyme activity in erythrocytes, but retain sufficient enzyme activity in leukocytes and other nucleated cells. OMIM: 102700
Date introduced: August 25, 2010
MeSH Unique ID: C531816
Heading Mapped to:
Entry Terms:
- Adenosine deaminase-deficient severe combined immunodeficiency disease
- ADA-SCID
- SCID Due to ADA Deficiency
- SCID Due to ADA Deficiency, Early-Onset
- Adenosine Deaminase Deficient Severe Combined Immunodeficiency
- Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due To Adenosine Deaminase Deficiency
- Severe combined immunodeficiency, alymphocytotic type
- Bubble boy disease
- Agammaglobulinemia, Swiss type
- SCID1
- Partial ADA Deficiency
- Partial adenosine deaminase deficiency
- Adenosine Deaminase Deficiency, Partial
- SCID Due to ADA Deficiency, Delayed Onset
- SCID Due to ADA Deficiency, Late-Onset
- Delayed-Late-Onset Adenosine Deaminase Deficiency
- Adenosine deaminase deficiency
- ADA Deficiency