infundibulopelvic stenosis-multicystic kidney syndrome GARD:0003005 Infundibulopelvic stenosis-multicystic kidney syndrome is a rare, genetic renal malformation syndrome characterized by variable degrees of malformation in the pelvicalyceal system (including unilateral or bilateral calyceal dilatation, infundibular stenosis, hypoplasia or stenosis of the renal pelvis) which lead to multicystic kidney. Clinically it exhibits abdominal, lumbar or flank pain, recurrent urinary tract infections, hypertension, proteinuria and often progresses to renal insufficiency. Calyceal dilatation and hydronephrosis are frequently seen on imaging. MESH:C535528 MONDO:0010971 OMIM:600989 Orphanet:1849 SCTID:725905005 UMLS:C1832949 infundibulopelvic dysgenesis syndromic renal or urinary tract malformation