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autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency

ORPHA: 319574

Contents

  1. 1. Available Treatments
  2. 2. Classification & Codes

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

Orphanet Code

ORPHA:319574
autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
OrphanetORPHA:319574
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO