Autosomal recessive hereditary disorder
Enzymopathy
Homocystinuria
Inherited disorder of folate metabolism
||||
Methylene tetrahydrofolate methyltransferase reductase deficiency AND homocystinuria (disorder)
Methylene THF reductase deficiency AND homocystinuria
Methylene tetrahydrofolate methyltransferase reductase deficiency AND homocystinuria
deficiëntie van methyleentetrahydrofolaatreductase en homocystinurie
Id28093001
StatusPrimitive
OccurrenceCongenital
ICD-10 complex map reference set
TargetE53.8
RuleTRUE
AdviceALWAYS E53.8
CorrelationSNOMED CT source code to target map code correlation not specified