Extrarenal Clinical Features are Reported for Most Genes Implicated in Genetic Kidney Disease.

Introduction: Genetic kidney disease is often suspected based on a family history of the disease or the presence of extrarenal features. This study examined how often a positive family history or syndromic features are found. Methods: A total of 255 genes from the Genomics England "green" lists for congenital anomalies of the kidney and urinary tract (CAKUT) ( Results: Autosomal recessive (AR) inheritance was recorded for 148 of the 248 genes (60%) with an OMIM entry. Extrarenal features were associated with 221 genes (89%), including those causing hematuria (5, 100%), renal ciliopathies (86, 97%), CAKUT (52, 91%), renal tubulopathies (41, 85%), and proteinuric renal diseases (37, 76%).The median number of affected systems was 4 (range: 0-10). More extrarenal features were associated with CAKUT (4, 0-10) and the ciliopathies (5, 0-9) than with hematuria (2, 2-5), proteinuria (3, 0-7), and the tubulopathies (3, 0-7) ( Conclusion: Extrarenal associations have been reported for most genes affected in genetic kidney disease, and are more common with pediatric-onset conditions with recessive inheritance. However, information is limited for how often extrarenal features are found in any individual.