BENTA disease
human disease
Facts
8 properties- Instance of
- rare disease, class of disease[2]
- Subclass of
- combined immunodeficiency, non-severe combined immunodeficiency[3][4]
- Age of onset
- infantile onset[8]
- Has phenotype
- splenomegaly, reinfection, immunoglobulin A deficiency, Lymphoid hyperplasia[9][10][11][12]
- Health specialty
- immunology[6]
- P14914
- D464336[13]
- Prevalence
- +0.000001[5]
🏷️ Also known as
en B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY
en B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA
en B-cell expansion with NF-kB and T-cell anergy disease
en BENTA
en BENTA disease
fr maladie BENTA
ja ベンタ病
🔖 Identifiers · 9
- Exact match
- www.orpha.net
- GARD rare disease ID
- 13339
- Microsoft Academic ID (discontinued)
- 2780211837
- Mondo ID
- MONDO_0014645
- OMIM ID
- 616452
- Orphanet ID
- 464336
- UMLS CUI
- CN231446
- UniProt disease ID
- DI-04476
- WikiProjectMed ID
- BENTA disease
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Summary
BENTA disease is a rare disease[1].