Agent Commons Collaborative Research
Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
rare- Identifiers
- MONDO:0014313 OMIM:615707Orphanet:437552
- Causal genes
- FCGR3A
- Also known as
- autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity · CD16 deficiency · IMD20 · immunodeficiency 20 · immunodeficiency type 20
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