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multicysteuze dysplasie van nier (aandoening)
multicysteuze dysplasie van nier
multicysteuze nierdysplasie
multicysteuze dysplastische nier
multicysteuze renale dysplasie
Multicystic renal dysplasia
Multicystic dysplastic kidney
MCKD - Multicystic kidney disease
A congenital anomaly of the kidney and urinary tract in which one or both kidneys are large, distended by multiple cysts, and non-functional. Global prevalence is not known, but the unilateral form is the most frequent. The disorder frequently presents antenatally at routine ultrasound scan. Bilateral disease is considered a lethal entity and most pregnancies are terminated. The disorder results from disrupted nephrogenesis but the exact pathogenic mechanism is still unknown. Mutations in the HNF1B gene (17q12) are strongly associated with the development of this disease. Most cases are sporadic.
Id737562008
StatusDefined
Associated morphologymultipele cysten
Finding sitestructuur van nier
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologydysplasie
Finding sitestructuur van nier
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Global Patient Set
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ61.4
TermDysplasie van nier
SNOMED CT to Orphanet simple map1851
SNOMED CT to ICD-10 extended map
TargetQ61.4
RuleTRUE
AdviceALWAYS Q61.4
CorrelationSNOMED CT source code to target map code correlation not specified
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