congenitaal nefrotisch syndroom WT1 mutatie (aandoening)
	congenitaal nefrotisch syndroom WT1 mutatie
	Congenital nephrotic syndrome due to WT-1 mutation

Id	22751000146108
Status	Primitive

Due to

Associated morphology	morfologische afwijking
Finding site	structuur van glomerulus
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	boven referentiebereik
Interprets	bepaling van eiwit in urine

Has interpretation	onder referentiebereik
Interprets	bepaling van albumine

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	N04.9
Term	Nefrotisch syndroom; niet gespecificeerd