Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder) (8707484)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder)
MAJOR CONCEPT File: 757, IEN: 7461950
DESIGNATION CODE
  • 3442833012
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE FULLY SPECIFIED NAME
SCOPE DIRECTLY LINKED
FORM FSN