autosomaal dominante hereditaire aandoening
familiaire aandoening
hereditair tumorpredispositiesyndroom
hereditaire aandoening van endocrien systeem
multinodulair struma
|||||
familiair multinodulair struma (aandoening)
familiair multinodulair struma
Familial multinodular goiter syndrome
Familial multinodular goiter
FMNG - familial multinodular goiter
A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors.
Id1279836009
StatusPrimitive
Associated morphologyvergroting
Finding sitegehele schildklier
Associated morphologymultinodulaire hyperplasie
Finding sitestructuur van schildklier
SNOMED CT to Orphanet simple map276399
SNOMED CT to ICD-10 extended map
TargetE04.2
RuleTRUE
AdviceALWAYS E04.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified