Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (8751334)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
MAJOR CONCEPT File: 757, IEN: 7461950
DESIGNATION CODE
  • 3442834018
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH