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encefalomyopathische vorm van syndroom van depletie van mitochondriaal deoxyribonucleïnezuur (aandoening)
encefalomyopathische vorm van syndroom van depletie van mitochondriaal deoxyribonucleïnezuur
encefalomyopathische vorm van mitochondriaal DNA-depletiesyndroom
Mitochondrial DNA depletion syndrome encephalomyopathic form
Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
A group of mitochondrial DNA maintenance syndrome diseases with characteristics of predominantly neuromuscular manifestations with typically infantile onset of hypotonia, lactic acidosis, psychomotor delay, progressive hyperkinetic-dystonic movement disorders, external ophthalmoplegia, sensorineural hearing loss, seizures and variable renal tubular dysfunction. It may be associated with a broad range of other clinical features.
Id765401006
StatusPrimitive
referentieset met complexe 'mapping' naar ICD-10
TargetE88.8
RuleTRUE
AdviceALWAYS E88.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
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