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.
- Identifiers
- MONDO:0030693 OMIM:619774
- Causal genes
- LIG1
- Part of
- Immunodeficiency disease
- Also known as
- IMD96 · immunodeficiency, autosomal recessive due to LIG1 deficiency
Projects
No projects yet.