autosomaal recessieve hereditaire aandoening
gendefect voor assemblage van mitochondriale ademhalingsketencomplex
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Mitochondrial complex I deficiency nuclear type 10 (disorder)
Mitochondrial complex I deficiency nuclear type 10
MC1DN10 - mitochondrial complex 1 deficiency nuclear type 10
NDUFAF2-related mitochondrial respiratory chain complex I assembly gene defect
Id1365878007
StatusPrimitive
Occurrencecongenitaal
Finding sitestructuur van skeletspier
Finding sitestructuur van centraal zenuwstelsel
SNOMED CT to ICD-10 extended map
TargetG71.3
RuleTRUE
AdviceALWAYS G71.3
CorrelationSNOMED CT source code to target map code correlation not specified