CAKUT2 (Q50349741)

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CAKUT that has material basis in heterozygous mutation in the TBX18 gene on chromosome 6q14
  • Ureteropelvic Junction Obstruction
  • Multicystic Renal Dysplasia, Bilateral
  • Pelviureteric Junction Obstruction
  • Hydronephrosis Due to Pujo
  • Congenital Anomalies of Kidney and Urinary Tract type 2
  • CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2
  • Congenital anomalies of the kidney and urinary tract 2
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Language Label Description Also known as
English
CAKUT2
CAKUT that has material basis in heterozygous mutation in the TBX18 gene on chromosome 6q14
  • Ureteropelvic Junction Obstruction
  • Multicystic Renal Dysplasia, Bilateral
  • Pelviureteric Junction Obstruction
  • Hydronephrosis Due to Pujo
  • Congenital Anomalies of Kidney and Urinary Tract type 2
  • CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2
  • Congenital anomalies of the kidney and urinary tract 2

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