autosomaal recessieve hereditaire aandoening
hereditaire aandoening van bewegingsapparaat
hereditaire aandoening van zenuwstelsel
hereditaire myopathie
mitochondriale encefalomyopathie
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'solute carrier family 25, member 42'-gerelateerde mitochondriale encefalomyopathie (aandoening)
SLC25A42-gerelateerde mitochondriale encefalomyopathie
'solute carrier family 25, member 42'-gerelateerde mitochondriale encefalomyopathie
SLC25A42 gene-related mitochondrial encephalomyopathy
SLC25A42-related mitochondrial coenzyme A transporter deficiency
Solute carrier family 25, member 42 gene-related mitochondrial encephalomyopathy
Id1388630003
StatusPrimitive
Finding sitestructuur van encephalon
Finding sitestructuur van skeletspier
SNOMED CT to ICD-10 extended map
TargetG71.3
RuleTRUE
AdviceALWAYS G71.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified