Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency (8751065)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency
MAJOR CONCEPT File: 757, IEN: 7461805
DESIGNATION CODE
  • 3442851013
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH