Autosomal recessive limb girdle muscular dystrophy due to desmin deficiency (8759593)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal recessive limb girdle muscular dystrophy due to desmin deficiency
MAJOR CONCEPT File: 757, IEN: 7468991
DESIGNATION CODE
  • 3467551017
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH
DEACTIVATION FLAG DEACTIVATED