Acute metabolic disorder	Acyl-CoA dehydrogenase deficiency	Autosomal dominant hereditary disorder	Neonatal metabolic disorder
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Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency (disorder)
	Transient neonatal multiple acyl-coenzyme A dehydrogenase deficiency
	Transient neonatal glutaric acidemia type 2 Transient neonatal MAD (multiple acyl-coenzyme A dehydrogenase) deficiency Transient neonatal multiple acyl-CoA dehydrogenase deficiency Transient neonatal glutaric aciduria type 2
	A very rare condition where a maternal riboflavin deficiency causes an infant to present with manifestations similar to those seen in multiple acyl-CoA dehydrogenase (MAD) deficiency such as poor suck, metabolic acidosis and hypoglycemia, but that resolves completely with oral riboflavin. In the one patient described haploinsufficiency of the human riboflavin transporter (hRFT1) was described in the mother.
	passagère neonatale glutaaracidurie type 2
	transiënte neonatale multipele acyl-CoA-dehydrogenasedeficiëntie passagère neonatale multipele deficiëntie van acyl-co-enzym-A-dehydrogenase passagère neonatale MADD

Id	723552005
Status	Primitive

Occurrence

Occurrence

Clinical course

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E71.3
Rule	TRUE
Advice	ALWAYS E71.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified