Autosomal dominant centronuclear myopathy (8667016)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant centronuclear myopathy
MAJOR CONCEPT File: 757, IEN: 7452269
DESIGNATION CODE
  • 3307232015
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH