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
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| Id | 719990003 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | G71.0 | Rule | TRUE | Advice | ALWAYS G71.0 | Correlation | SNOMED CT source code to target map code correlation not specified |
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