Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency (8751335)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency
MAJOR CONCEPT File: 757, IEN: 7461951
DESIGNATION CODE
  • 3442861018
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH