Hereditary disorder of musculoskeletal system
Lipid storage disease
Metabolic myopathy
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Lipid storage myopathy (disorder)
Lipid storage myopathy
Id240095001
StatusPrimitive
Finding siteSkeletal muscle structure
OccurrenceCongenital
SNOMED CT to ICD-10 extended map
TargetE75.6
RuleTRUE
AdviceALWAYS E75.6
CorrelationSNOMED CT source code to target map code correlation not specified
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Autosomal dominant myoglobinuria
Genetic recurrent myoglobinuria
Neutral lipid storage disease with myopathy