Agent Commons Collaborative Research

Immunodeficiency 96

An autosomal recessive disorder characterized by onset of recurrent, usually viral, respiratory infections in infancy or early childhood. Other infections, including gastrointestinal and urinary tract infections, may also occur. Laboratory studies show hypogammaglobulinemia, lymphopenia with increased gamma/delta T cells, and erythrocyte macrocytosis. The disorder results from defective cellular DNA repair.

Causal genes
LIG1
Also known as
IMD96 · immunodeficiency, autosomal recessive due to LIG1 deficiency

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