hereditaire aandoening van bewegingsapparaat
hereditaire myopathie
mitochondriale myopathie
X-gebonden hereditaire aandoening
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Apoptosis inducing factor mitochondria associated 1 gene related X-linked mitochondrial myopathy (disorder)
AIFM1 gene related X-linked mitochondrial myopathy
AIFM1 related X-linked mitochondrial myopathy
Apoptosis inducing factor mitochondria associated 1 gene related X-linked mitochondrial myopathy
Id1406999008
StatusPrimitive
Finding sitestructuur van skeletspier
SNOMED CT to ICD-10 extended map
TargetG71.3
RuleTRUE
AdviceALWAYS G71.3
CorrelationSNOMED CT source code to target map code correlation not specified
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ernstige X-gebonden mitochondriale encefalomyopathie