Disease - Congenital anomalies of kidney and urinary tract 2
- DefinitionA disorder encompassing a broad spectrum of renal and urinary tract malformations that include renal agenesis, kidney hypodysplasia, multicystic kidney dysplasia, duplex collecting system, posterior urethral valves and ureter abnormalities. Congenital anomalies of kidney and urinary tract are the commonest cause of chronic kidney disease in children.
- AcronymCAKUT2
- Alternative names
- Cross references
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Browse 1 entry- T-box transcription factor TBX18 · Gene: TBX18 · Homo sapiens (Human) · 607 amino acids · Evidence at protein level · Annotation score: 5/5