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deficiëntie van mitochondriaal complex I door deficiëntie van acyl-co-enzym A-dehydrogenase 9 (aandoening)
deficiëntie van mitochondriaal complex I door deficiëntie van acyl-co-enzym A-dehydrogenase 9
mitochondriaal-complex I-deficiëntie door ACAD9-deficiëntie
mitochondriaal-complex I-deficiëntie door acyl-CoA-dehydrogenase 9-deficiëntie
Acyl-CoA dehydrogenase 9 deficiency
Deficiency of acyl-coenzyme A dehydrogenase 9
ACAD9 (acyl-CoA dehydrogenase 9) deficiency
Mitochondrial complex I deficiency due to deficiency of acyl-coenzyme A dehydrogenase 9
A rare disorder characterized by neurological dysfunction, hepatic failure and cardiomyopathy due to a deficiency of complex I of the respiratory chain.
Id725046003
StatusPrimitive
Occurrencecongenitaal
DHD Diagnosis thesaurus reference set
SNOMED CT to Orphanet simple map99901
SNOMED CT to ICD-10 extended map
TargetE71.3
RuleTRUE
AdviceALWAYS E71.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified