Autosomal dominant hereditary disorder
Thyroxine transport defect
||
Autosomal dominant variant form of albumin (disorder)
Autosomal dominant variant form of albumin
autosomaal dominante variante vorm van albumine
Id21367009
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