Immunodeficiency 19
Also known as CD3D, CD3D severe combined immunodeficiency (disease), CD3delta deficiency, immunodeficiency type 19+5 more
CD3D, CD3D severe combined immunodeficiency (disease), CD3delta deficiency, immunodeficiency type 19, severe combined immunodeficiency (disease) caused by mutation in CD3D, CD3-Delta deficiency, IMD19, SCID, T cell-negative, B cell-positive, NK cell-positive, severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive.
What's happening now
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.
CD3D, CD3D severe combined immunodeficiency (disease), CD3delta deficiency, immunodeficiency type 19, severe combined immunodeficiency (disease) caused by mutation in CD3D, CD3-Delta deficiency, IMD19, SCID, T cell-negative, B cell-positive, NK cell-positive, severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.