autosomal recessive disease rare syndrome with cardiac malformations syndromic urogenital tract malformation syndromic genetic deafness syndromic renal or urinary tract malformation congenital vertebral-cardiac-renal anomalies syndrome MONDO:0020831 OMIMPS:617660 Orphanet:521438 VCRL vertebral, cardiac, renal, and limb defects syndrome genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability