Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder) (8707194)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder)
MAJOR CONCEPT File: 757, IEN: 7461805
DESIGNATION CODE
  • 3442849014
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE FULLY SPECIFIED NAME
SCOPE DIRECTLY LINKED
FORM FSN