Benign autosomal dominant myopathy (8695802)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Benign autosomal dominant myopathy
MAJOR CONCEPT File: 757, IEN: 7454558
DESIGNATION CODE
  • 3312804019
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH