autosomaal dominante polycysteuze nierziekte (aandoening)
autosomaal dominante polycysteuze nierziekte
autosomaal dominante cystenieren
autosomaal dominante polycysteuze nierziekte
Autosomaal dominante polycysteuze nierziekte; vorm van cystenieren die autosomaal dominant overerft, dat wil zeggen dat iemand 50% kans heeft dat hij de aanleg erft indien een van de ouders de ziekte heeft.
Autosomal dominant polycystic kidney disease
ADPKD - autosomal dominant polycystic kidney disease
Inherited disease with characteristics of the development of cysts in the kidneys. The disease rarely causes any noticeable problems until the cysts grow large enough to affect renal function, usually between 30 and 60 years of age. Less commonly, children or older people may have noticeable symptoms. Two different genes are known to cause this disease PKD1 and PKD2.
Associated morphologypolycysteuze verandering
Finding sitestructuur van nier
Global Patient Set
International Patient Summary
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TermPolycystische nier, autosomaal dominant
SNOMED CT to Orphanet simple map730
SNOMED CT to MedDRA simple map10036046
SNOMED CT to ICD-10 extended map
AdviceALWAYS Q61.2
CorrelationSNOMED CT source code to target map code correlation not specified