Autosomal recessive hereditary disorder	Autosomal recessive hereditary disorder	Disorder of glycine metabolism	Disorder of glycine metabolism	Hereditary metabolic disease	Specific enzyme deficiency	Specific enzyme deficiency
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Deficiency of dimethylglycine dehydrogenase (disorder)
	Deficiency of dimethylglycine dehydrogenase
	Dimethylglycine dehydrogenase deficiency
	An extremely rare autosomal recessive glycine metabolism disorder characterized clinically in the single reported case to date by muscle fatigue and a fish-like odor.
	deficiëntie van dimethylglycinedehydrogenase
	dimethylglycinedehydrogenasedeficiëntie

Id	719449007
Status	Primitive

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E72.5
Rule	TRUE
Advice	ALWAYS E72.5
Correlation	SNOMED CT source code to target map code correlation not specified