Congenital hypothyroidism
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Congenital hypothyroidism due to symporter mutation (disorder)
Congenital hypothyroidism due to symporter mutation
Id1179397005
StatusPrimitive
Finding siteThyroid structure
OccurrenceCongenital
SNOMED CT to ICD-10 extended map
TargetE03.0
RuleTRUE
AdviceALWAYS E03.0
CorrelationSNOMED CT source code to target map code correlation not specified