autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
ORPHA: 319589
Available Treatments (0)
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Classification & Codes
Orphanet Code
ORPHA:319589autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
| Orphanet | ORPHA:319589 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO