Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency (8751333)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency
MAJOR CONCEPT File: 757, IEN: 7461950
DESIGNATION CODE
  • 3442835017
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH