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Autosomal dominant limb girdle muscular dystrophy type 1G (disorder)
Autosomal dominant limb girdle muscular dystrophy type 1G
A mild form of limb girdle muscular dystrophy that has characteristics of limb-girdle weakness, marked proximal amyotrophy and abolished myotatic reflexes, associated with progressive fingers and toes flexion limitation.
autosomaal dominante 'limb-girdle'-spierdystrofie type 1G
LGMD1G
autosomaal dominante gordeldystrofie type 1G
autosomaal dominante 'limb-girdle muscular dystrophy' type 1G
Id719990003
StatusPrimitive
Associated morphologyDystrophy
Finding siteSkeletal muscle structure
Pathological processPathological developmental process
Clinical courseProgressive
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG71.0
RuleTRUE
AdviceALWAYS G71.0
CorrelationSNOMED CT source code to target map code correlation not specified