has material basis in germline mutation in PBX1 hereditary disease congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay https://www.malacards.org/card/congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss_abnormal_ears_or_developmental_delay DOID:0112359 CAKUTHED UMLS:C4539968 GARD:0025998 congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay MONDO:0060549 OMIM:617641 Orphanet:656130 MEDGEN:1612119