C176821Level 7
Immunodeficiency 48
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal recessive immunodeficiency caused by mutation(s) in the ZAP70 gene, encoding tyrosine-protein kinase ZAP-70. It is characterized by absent CD8+ cells.
**Synonyms:** - STCD - Selective T-Cell Defect - ZAP 70 deficiency
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