autosomaal dominante hereditaire aandoening	hereditaire nefropathie	hyperurikemie	renale tubulopathie	uraatnefropathie
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syndroom van hyperurikemie, anemie en nierfalen (aandoening)
	syndroom van hyperurikemie, anemie en nierfalen
	syndroom van hyperurikemie, bloedarmoede en nierinsufficiëntie
	Hyperuricemia, anemia, renal failure syndrome
	Familial juvenile hyperuricemic nephropathy type 2 Renin associated familial juvenile hyperuricemic nephropathy
	A rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system.

Id	721840000
Status	Primitive

Causative agent	uraat
Finding site	structuur van tubulus renalis

SNOMED CT to Orphanet simple map

217330

SNOMED CT to ICD-10 extended map

Target	E79.0
Rule	TRUE
Advice	ALWAYS E79.0
Correlation	SNOMED CT source code to target map code correlation not specified

Target	D61.9
Rule	TRUE
Advice	ALWAYS D61.9
Correlation	SNOMED CT source code to target map code correlation not specified

Target	N19
Rule	TRUE
Advice	ALWAYS N19
Correlation	SNOMED CT source code to target map code correlation not specified