Autosomal dominant hereditary disorder	Congenital anomaly of the kidney	Congenital anomaly of the urinary tract proper	Developmental hereditary disorder	Hereditary nephropathy
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Infundibulopelvic stenosis multicystic kidney syndrome (disorder)
	Infundibulopelvic stenosis multicystic kidney syndrome
	Infundibulopelvic dysgenesis
	syndroom van infundibulopelvisstenose en multicysteuze nier

Id	725905005
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Renal collecting system structure
Occurrence	Congenital
Pathological process	Pathological developmental process

ICD-10 complex map reference set

Target	Q63.8
Rule	TRUE
Advice	ALWAYS Q63.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified