Congenital disease
Hereditary disorder of endocrine system
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Homozygous methylenetetrahydrofolate reductase mutation (disorder)
Homozygous methylenetetrahydrofolate reductase mutation
homozygote mutatie van methyleentetrahydrofolaatreductase-gen
homozygote MTHFR-mutatie
Id139811000119109
StatusPrimitive
Finding siteStructure of endocrine system
OccurrenceCongenital
ICD-10 complex map reference set
TargetE72.1
RuleTRUE
AdviceALWAYS E72.1
CorrelationSNOMED CT source code to target map code correlation not specified