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laat optredende glycogeenstapelingsziekte type II (aandoening)
laat optredende glycogeenstapelingsziekte type II
Glycogen storage disease due to acid maltase deficiency, late-onset
Glycogenosis type II, late onset
Alpha-1,4-glucosidase acid deficiency, late onset
Glycogen storage disease type II late onset
Pompe disease, late onset
Glycogen storage disease due to acid maltase deficiency, late onset (AMDL), a form of Glycogen storage disease due to acid maltase deficiency (AMD), a degenerative metabolic myopathy particularly affecting respiratory and skeletal muscles, is characterized by an accumulation of glycogen in lysosomes.
Id722343009
StatusPrimitive
Occurrencecongenitaal
referentieset met complexe 'mapping' naar ICD-10
TargetE74.0
RuleTRUE
AdviceALWAYS E74.0
CorrelationSNOMED CT source code to target map code correlation not specified