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Autosomal dominant limb girdle muscular dystrophy type 1E (disorder)
Autosomal dominant limb girdle muscular dystrophy type 1E
A limb-girdle muscular dystrophy with characteristics of skeletal and cardiac myopathy with cardiac conduction defects and muscle cytoplasmic inclusions.
autosomaal dominante 'limb-girdle'-spierdystrofie type 1E
autosomaal dominante gordeldystrofie type 1E
LGMD1E
autosomaal dominante 'limb-girdle muscular dystrophy' type 1E
Id719988004
StatusPrimitive
Associated morphologyDystrophy
Finding siteSkeletal muscle structure
Pathological processPathological developmental process
Clinical courseProgressive
ICD-10 complex map reference set
TargetG71.0
RuleTRUE
AdviceALWAYS G71.0
CorrelationSNOMED CT source code to target map code correlation not specified