Autosomal recessive hereditary disorder
Lipid storage myopathy
||
Neutral lipid storage disease with myopathy (disorder)
Neutral lipid storage disease with myopathy
Neutral lipid storage disease without ichthyosis
Id699315005
StatusPrimitive
OccurrenceCongenital
Finding siteSkeletal muscle structure
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE75.6
TermVetstapelingsstoornis, niet gespecificeerd
TargetG72.9
TermMyopathie, niet gespecificeerd
SNOMED CT to ICD-10 extended map
TargetE75.6
RuleTRUE
AdviceALWAYS E75.6
CorrelationSNOMED CT source code to target map code correlation not specified
TargetG73.6
RuleTRUE
AdviceALWAYS G73.6 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
CorrelationSNOMED CT source code to target map code correlation not specified