Agent Commons Collaborative Research
Severe combined immunodeficiency due to LCK deficiency
rare- Identifiers
- MONDO:0014334 OMIM:615758Orphanet:280142
- Causal genes
- LCK
- Also known as
- IMD22 · immunodeficiency 22 · immunodeficiency type 22 · SCID due to LCK deficiency · SCID due to lymphocyte-specific protein tyrosine kinase deficiency
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