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familiaire hyperthyreoïdie door mutatie in thyrotropinereceptor (aandoening)
familiaire hyperthyreoïdie door mutatie in thyrotropinereceptor
familiaire hyperthyroïdie door mutatie in TSH-receptor
familiaire niet-immune hyperthyroïdie
Familial non-autoimmune autosomal dominant hyperthyroidism
Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor
Familial non-immune hyperthyroidism
A rare hyperthyroidism characterized by mild to severe hyperthyroidism, presence of goiter, absence of features of autoimmunity, frequent relapses while on treatment and a positive family history.
Id716743006
StatusPrimitive
DHD Diagnosis thesaurus reference set
SNOMED CT to Orphanet simple map424
SNOMED CT to ICD-10 extended map
TargetE05.8
RuleTRUE
AdviceALWAYS E05.8
CorrelationSNOMED CT source code to target map code correlation not specified