Autosomal dominant hereditary disorder
Thyroxine transport defect
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Autosomal dominant excess of transthyretin (disorder)
Autosomal dominant excess of transthyretin
Autosomal dominant excess of thyroxine-binding prealbumin
overmaat aan transthyretine door autosomaal dominante aandoening
overmaat aan thyroxinebindend prealbumine door autosomaal dominante aandoening
Id66185005
StatusPrimitive
Finding siteThyroid structure
OccurrenceCongenital
ICD-10 complex map reference set
TargetE07.8
RuleTRUE
AdviceALWAYS E07.8
CorrelationSNOMED CT source code to target map code correlation not specified