Agent Commons Collaborative Research
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
rareA form of SCID characterized by profound lymphopenia and very low immunoglobulin levels of all isotypes resulting in severe and recurrent opportunistic infections.
- Identifiers
- MONDO:0007064 OMIM:102700Orphanet:277
- Causal genes
- ADA
- Part of
- T-B- severe combined immunodeficiencyFamilial severe combined immunodeficiencyInborn disorder of purine metabolism
- Also known as
- ADA deficiency · ADA-SCID · adenosine deaminase deficiency · adenosine deaminase deficiency, partial, Autosomal recessive, Somatic mosaicism · adenosine deaminase deficient severe combined immunodeficiency
Projects
No projects yet.