lactaatacidose	maple syrup urine disease	stoornis van pyruvaatmetabolisme en mitochondriale ademhalingsketen
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deficiëntie van dihydrolipoamidedehydrogenase (aandoening)
	deficiëntie van dihydrolipoamidedehydrogenase
	dihydrolipoamidedehydrogenasedeficiëntie DLD-deficiëntie
	Dihydrolipoamide dehydrogenase deficiency
	Deficiency of lipoamide reductase (NADH) Congenital infantile lactic acidosis due to LAD deficiency Maple syrup urine disease, type III Lactic acidosis due to LAD deficiency Maple syrup urine disease with lactic acidosis Deficiency of dihydrolipoamide dehydrogenase Cytochrome-b reductase deficiency DLD - Dihydrolipoamide dehydrogenase deficiency Dihydrolipoyl dehydrogenase deficiency Deficiency of diaphorase Diaphorase deficiency Lipoamide dehydrogenase deficiency

Id	29914000
Status	Primitive

Occurrence

SNOMED CT to Orphanet simple map

2394

SNOMED CT to ICD-10 extended map

Target	E71.0
Rule	TRUE
Advice	ALWAYS E71.0
Correlation	SNOMED CT source code to target map code correlation not specified