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congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal dominant disorder characterized by variable congenital anomalies of the kidney and urinary tract, sometimes resulting in renal dysfunction or failure, dysmorphic facial features, and abnormalities of the outer ear. Most patients have hearing loss, and some may have global developmental delay.
Mondo Term and Equivalent IDs
MONDO:0060549:  congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay
UMLS:C4539968: