IFNGR2
interferon gamma receptor 2
Ассоциированные заболевания
Герминативная мутация (причина)3
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiencyORPHA:319547
→Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiencyORPHA:319589
→Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiencyORPHA:319574
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