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syndroom van hyperurikemie, anemie en nierfalen (aandoening)
syndroom van hyperurikemie, anemie en nierfalen
syndroom van hyperurikemie, bloedarmoede en nierinsufficiƫntie
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.
Id721840000
StatusPrimitive
Causative agenturaat
Finding sitestructuur van tubulus renalis
SNOMED CT to Orphanet simple map217330
SNOMED CT to ICD-10 extended map
TargetE79.0
RuleTRUE
AdviceALWAYS E79.0
CorrelationSNOMED CT source code to target map code correlation not specified
TargetD61.9
RuleTRUE
AdviceALWAYS D61.9
CorrelationSNOMED CT source code to target map code correlation not specified
TargetN19
RuleTRUE
AdviceALWAYS N19
CorrelationSNOMED CT source code to target map code correlation not specified