carnitinedeficiëntie door aangeboren defect van stofwisseling
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Epsilon-N-trimethyllysine hydroxylase carnitine deficiency disorder (disorder)
Epsilon-N-trimethyllysine hydroxylase carnitine deficiency disorder
TMLHE gene related carnitine deficiency disorder
Id1366322006
StatusPrimitive
Due toaangeboren defect van stofwisseling
Occurrencecongenitaal
SNOMED CT to ICD-10 extended map
TargetE71.3
RuleTRUE
AdviceALWAYS E71.3
CorrelationSNOMED CT source code to target map code correlation not specified