Autosomal recessive hereditary disorder
Enzymopathy
Inborn error of metabolism
Non-ketotic hyperglycinemia
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Glycine dehydrogenase (decarboxylating) deficiency (disorder)
Glycine dehydrogenase (decarboxylating) deficiency
Non-ketotic hyperglycinemia type I
P protein deficiency
Glycine dehydrogenase decarboxylating deficiency
Glycine decarboxylase deficiency
Non-ketotic hyperglycinemia P protein deficiency
P-protein deficiency
Nonketotic hyperglycinemia, type I
Id63329001
StatusPrimitive
OccurrenceCongenital
SNOMED CT to ICD-10 extended map
TargetE72.5
RuleTRUE
AdviceALWAYS E72.5
CorrelationSNOMED CT source code to target map code correlation not specified