Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
Also known as CD16 deficiency, autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity, immunodeficiency type 20, IMD20+1 more
CD16 deficiency, autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity, immunodeficiency type 20, IMD20, immunodeficiency 20.
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An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
CD16 deficiency, autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity, immunodeficiency type 20, IMD20, immunodeficiency 20
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.