Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
---|
HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ACTG2 CL E G H | 72 | 145 | ORPHA:2604 | Familial visceral myopathy | HP:0040281 - Very frequent | | | 23 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ACTG2 CL E G H | 72 | 145 | OMIM:155310 | Visceral myopathy 1 | . | | | 23 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | AFF4 CL E G H | 27125 | 17869 | OMIM:616368 | CHOPS syndrome | . | | | 6 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | AFF4 CL E G H | 27125 | 17869 | ORPHA:444077 | Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome | HP:0040283 - Occasional | | | 6 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ANKLE2 CL E G H | 23141 | 29101 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 3 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | APC2 CL E G H | 10297 | 24036 | ORPHA:821 | Sotos syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ARNT2 CL E G H | 9915 | 16876 | OMIM:615926 | Webb-Dattani syndrome | . | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ARVCF CL E G H | 421 | 728 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ASPM CL E G H | 259266 | 19048 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 512 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ASXL1 CL E G H | 171023 | 18318 | OMIM:605039 | Bohring-Opitz syndrome | . | | | 145 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ATRX CL E G H | 546 | 886 | OMIM:309580 | Mental retardation-hypotonic facies syndrome, X-linked, 1 | . | | | 169 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | BAZ1B CL E G H | 9031 | 961 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | BCL7B CL E G H | 9275 | 1005 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | BICC1 CL E G H | 80114 | 19351 | OMIM:601331 | Renal dysplasia, cystic, susceptibility to | HP:0040283 - Occasional | | | 5 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | BNC2 CL E G H | 54796 | 30988 | OMIM:618612 | LOWER URINARY TRACT OBSTRUCTION, CONGENITAL; LUTO | | | | 22 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | BNC2 CL E G H | 54796 | 30988 | ORPHA:93110 | Posterior urethral valve | HP:0040282 - Frequent | | | 22 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | BPTF CL E G H | 2186 | 3581 | ORPHA:529962 | 17q24.2 microdeletion syndrome | HP:0040284 - Very rare | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | BRD4 CL E G H | 23476 | 13575 | ORPHA:199 | Cornelia de Lange syndrome | HP:0040282 - Frequent | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | BUD23 CL E G H | 114049 | 16405 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CCBE1 CL E G H | 147372 | 29426 | OMIM:235510 | Hennekam lymphangiectasia-lymphedema syndrome | . | | | 147 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CCNQ CL E G H | 92002 | 28434 | ORPHA:140952 | Syndactyly-telecanthus-anogenital and renal malformations syndrome | HP:0040282 - Frequent | | | 7 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CCNQ CL E G H | 92002 | 28434 | OMIM:300707 | Toe syndactyly, telecanthus, and anogenital and renal malformations | . | | | 7 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CDC45 CL E G H | 8318 | 1739 | OMIM:617063 | Meier-Gorlin syndrome 7 | . | | | 9 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CDK5RAP2 CL E G H | 55755 | 18672 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 181 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CDK6 CL E G H | 1021 | 1777 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 6 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CDKN1C CL E G H | 1028 | 1786 | OMIM:130650 | Beckwith-Wiedemann syndrome | . | | | 114 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CENPJ CL E G H | 55835 | 17272 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 161 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CEP135 CL E G H | 9662 | 29086 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 38 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CEP152 CL E G H | 22995 | 29298 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 146 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CEP63 CL E G H | 80254 | 25815 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 31 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CHD4 CL E G H | 1108 | 1919 | OMIM:617159 | Sifrim-Hitz-Weiss syndrome | . | | | 14 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CHD7 CL E G H | 55636 | 20626 | ORPHA:138 | CHARGE syndrome | HP:0040283 - Occasional | | | 515 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CHRM3 CL E G H | 1131 | 1952 | ORPHA:2970 | Prune belly syndrome | HP:0040281 - Very frequent | | | 4 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CHRNA3 CL E G H | 1136 | 1957 | OMIM:191800 | URINARY BLADDER, ATONY OF | | | | 4 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CIT CL E G H | 11113 | 1985 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 15 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CLIP2 CL E G H | 7461 | 2586 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | COL18A1 CL E G H | 80781 | 2195 | ORPHA:1571 | Knobloch syndrome | HP:0040283 - Occasional | | | 177 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | COMT CL E G H | 1312 | 2228 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | 6 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | COPB2 CL E G H | 9276 | 2232 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CREBBP CL E G H | 1387 | 2348 | ORPHA:353281 | Rubinstein-Taybi syndrome due to 16p13.3 microdeletion | HP:0040283 - Occasional | | | 291 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | CREBBP CL E G H | 1387 | 2348 | ORPHA:353277 | Rubinstein-Taybi syndrome due to CREBBP mutations | HP:0040283 - Occasional | | | 291 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | DACT1 CL E G H | 51339 | 17748 | ORPHA:857 | Townes-Brocks syndrome | HP:0040283 - Occasional | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | DCDC2 CL E G H | 51473 | 18141 | OMIM:617394 | Sclerosing cholangitis, neonatal | | | | 8 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | DDX6 CL E G H | 1656 | 2747 | OMIM:618653 | INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES; IDDILF | | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | DNAJC30 CL E G H | 84277 | 16410 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | DNMT3A CL E G H | 1788 | 2978 | OMIM:615879 | Tatton-Brown-Rahman syndrome | | | | 44 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | DSTYK CL E G H | 25778 | 29043 | OMIM:610805 | Congenital anomalies of kidney and urinary tract, susceptibility to | . | | | 13 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | DVL3 CL E G H | 1857 | 3087 | OMIM:616894 | ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3; DRS3 | | | | 5 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EBF3 CL E G H | 253738 | 19087 | OMIM:617330 | HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS | | | | 25 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EFEMP2 CL E G H | 30008 | 3219 | ORPHA:90349 | Autosomal recessive cutis laxa type 1 | HP:0040283 - Occasional | | | 45 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EHMT1 CL E G H | 79813 | 24650 | ORPHA:96147 | Kleefstra syndrome due to 9q34 microdeletion | HP:0040283 - Occasional | | | 223 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EHMT1 CL E G H | 79813 | 24650 | ORPHA:261652 | Kleefstra syndrome due to a point mutation | HP:0040283 - Occasional | | | 223 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EIF4H CL E G H | 7458 | 12741 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ELN CL E G H | 2006 | 3327 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 172 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ELN CL E G H | 2006 | 3327 | OMIM:194050 | Williams-Beuren syndrome | . | | | 172 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EP300 CL E G H | 2033 | 3373 | ORPHA:353284 | Rubinstein-Taybi syndrome due to EP300 haploinsufficiency | HP:0040283 - Occasional | | | 250 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EXT1 CL E G H | 2131 | 3512 | ORPHA:502 | Trichorhinophalangeal syndrome type 2 | HP:0040283 - Occasional | | | 96 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EYA1 CL E G H | 2138 | 3519 | ORPHA:107 | BOR syndrome | HP:0040283 - Occasional | | | 135 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | EYA1 CL E G H | 2138 | 3519 | OMIM:113650 | Branchiootorenal syndrome 1 | . | | | 135 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FANCF CL E G H | 2188 | 3587 | OMIM:603467 | FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF | | | | 87 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FANCI CL E G H | 55215 | 25568 | OMIM:609053 | Fanconi anemia, complementation group I | . | | | 157 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FBLN5 CL E G H | 10516 | 3602 | ORPHA:90349 | Autosomal recessive cutis laxa type 1 | HP:0040283 - Occasional | | | 63 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FGF10 CL E G H | 2255 | 3666 | ORPHA:2363 | Lacrimoauriculodentodigital syndrome | HP:0040284 - Very rare | | | 17 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FGFR2 CL E G H | 2263 | 3689 | ORPHA:2363 | Lacrimoauriculodentodigital syndrome | HP:0040284 - Very rare | | | 175 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FGFR2 CL E G H | 2263 | 3689 | ORPHA:93260 | Pfeiffer syndrome type 3 | HP:0040283 - Occasional | | | 175 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FGFR3 CL E G H | 2261 | 3690 | ORPHA:2363 | Lacrimoauriculodentodigital syndrome | HP:0040284 - Very rare | | | 145 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FKBP6 CL E G H | 8468 | 3722 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FLNA CL E G H | 2316 | 3754 | ORPHA:2484 | Melnick-Needles syndrome | HP:0040282 - Frequent | | | 493 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | FUZ CL E G H | 80199 | 26219 | ORPHA:3027 | Caudal regression sequence | HP:0040282 - Frequent | | | 3 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | GATA3 CL E G H | 2625 | 4172 | ORPHA:2237 | Hypoparathyroidism-sensorineural deafness-renal disease syndrome | HP:0040282 - Frequent | | | 83 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | GP1BB CL E G H | 2812 | 4440 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | 8 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | GREB1L CL E G H | 80000 | 31042 | OMIM:617805 | Renal hypodysplasia/aplasia 3 | HP:0040284 - Very rare | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | GTF2I CL E G H | 2969 | 4659 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | GTF2IRD1 CL E G H | 9569 | 4661 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | GTF2IRD2 CL E G H | 84163 | 30775 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | H19-ICR CL E G H | 105259599 | | OMIM:130650 | Beckwith-Wiedemann syndrome | . | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | H4C9 CL E G H | 8294 | 4793 | OMIM:619951 | | | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HAAO CL E G H | 23498 | 4796 | OMIM:617660 | Vertebral, cardiac, renal, and limb defects syndrome 1 | . | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HDAC8 CL E G H | 55869 | 13315 | ORPHA:199 | Cornelia de Lange syndrome | HP:0040282 - Frequent | | | 37 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HIRA CL E G H | 7290 | 4916 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | 3 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HNRNPK CL E G H | 3190 | 5044 | ORPHA:352665 | Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to 9q21.3 microdeletion | HP:0040282 - Frequent | | | 8 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HNRNPK CL E G H | 3190 | 5044 | ORPHA:453504 | Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome due to a point mutation | HP:0040282 - Frequent | | | 8 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HNRNPU CL E G H | 3192 | 5048 | ORPHA:238769 | 1q44 microdeletion syndrome | HP:0040283 - Occasional | | | 39 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HOXA13 CL E G H | 3209 | 5102 | OMIM:140000 | Hand-Foot-Genital syndrome | . | | | 11 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HOXA13 CL E G H | 3209 | 5102 | ORPHA:2438 | Hand-foot-genital syndrome | HP:0040282 - Frequent | | | 11 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HPSE2 CL E G H | 60495 | 18374 | ORPHA:2704 | Ochoa syndrome | HP:0040282 - Frequent | | | 9 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | HSPA9 CL E G H | 3313 | 5244 | OMIM:616854 | Even-Plus syndrome | | | | 6 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | IGF2 CL E G H | 3481 | 5466 | OMIM:130650 | Beckwith-Wiedemann syndrome | . | | | 9 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ISL1 CL E G H | 3670 | 6132 | ORPHA:93930 | Bladder exstrophy | HP:0040281 - Very frequent | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | JAG1 CL E G H | 182 | 6188 | OMIM:118450 | Alagille syndrome 1 | | | | 257 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | JMJD1C CL E G H | 221037 | 12313 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KANSL1 CL E G H | 284058 | 24565 | ORPHA:363958 | 17q21.31 microdeletion syndrome | HP:0040283 - Occasional | | | 283 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KANSL1 CL E G H | 284058 | 24565 | OMIM:610443 | Koolen-De Vries syndrome | | | | 283 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KANSL1 CL E G H | 284058 | 24565 | ORPHA:363965 | Koolen-De Vries syndrome due to a point mutation | HP:0040283 - Occasional | | | 283 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KAT5 CL E G H | 10524 | 5275 | OMIM:619103 | NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB | | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:130650 | Beckwith-Wiedemann syndrome | . | | | 730 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KCNQ1OT1 CL E G H | 10984 | 6295 | OMIM:130650 | Beckwith-Wiedemann syndrome | . | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KIF14 CL E G H | 9928 | 19181 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 9 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KMT2C CL E G H | 58508 | 13726 | ORPHA:261652 | Kleefstra syndrome due to a point mutation | HP:0040283 - Occasional | | | 99 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | KNL1 CL E G H | 57082 | 24054 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 112 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | LIMK1 CL E G H | 3984 | 6613 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | LRIG2 CL E G H | 9860 | 20889 | ORPHA:2704 | Ochoa syndrome | HP:0040282 - Frequent | | | 5 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | LRIG2 CL E G H | 9860 | 20889 | OMIM:615112 | Urofacial syndrome 2 | . | | | 5 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | LTBP1 CL E G H | 4052 | 6714 | ORPHA:90349 | Autosomal recessive cutis laxa type 1 | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MAP3K7 CL E G H | 6885 | 6859 | OMIM:157800 | Cardiospondylocarpofacial syndrome | . | | | 11 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MAPKAPK5 CL E G H | 8550 | 6889 | OMIM:619869 | | | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MBTPS2 CL E G H | 51360 | 15455 | ORPHA:85284 | BRESEK syndrome | HP:0040282 - Frequent | | | 22 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MCM7 CL E G H | 4176 | 6950 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MCPH1 CL E G H | 79648 | 6954 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 155 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MED12 CL E G H | 9968 | 11957 | OMIM:301068 | HARDIKAR SYNDROME; HDKR | | | | 228 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | METTL27 CL E G H | 155368 | 19068 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | METTL5 CL E G H | 29081 | 25006 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MFSD2A CL E G H | 84879 | 25897 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 5 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MID1 CL E G H | 4281 | 7095 | ORPHA:2745 | Opitz GBBB syndrome | HP:0040283 - Occasional | | | 57 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MID1 CL E G H | 4281 | 7095 | OMIM:300000 | Opitz gbbb syndrome, type I | | | | 57 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MLXIPL CL E G H | 51085 | 12744 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MLXIPL CL E G H | 51085 | 12744 | OMIM:194050 | Williams-Beuren syndrome | . | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MNX1 CL E G H | 3110 | 4979 | ORPHA:1552 | Currarino syndrome | HP:0040283 - Occasional | | | 17 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MNX1 CL E G H | 3110 | 4979 | OMIM:176450 | Currarino syndrome | . | | | 17 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | MYCN CL E G H | 4613 | 7559 | ORPHA:391641 | Feingold syndrome type 1 | HP:0040283 - Occasional | | | 35 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NCAPD3 CL E G H | 23310 | 28952 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NCAPG2 CL E G H | 54892 | 21904 | OMIM:618460 | Khan-Khan-Katsanis syndrome | . | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NCF1 CL E G H | 653361 | 7660 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 13 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NFIA CL E G H | 4774 | 7784 | OMIM:613735 | Brain malformations with or without urinary tract defects | HP:0040282 - Frequent | | | 12 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NIPBL CL E G H | 25836 | 28862 | ORPHA:199 | Cornelia de Lange syndrome | HP:0040282 - Frequent | | | 494 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NIPBL CL E G H | 25836 | 28862 | OMIM:122470 | Cornelia de Lange syndrome 1 | HP:0040283 - Occasional | | | 494 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NKX2-1 CL E G H | 7080 | 11825 | ORPHA:209905 | Brain-lung-thyroid syndrome | HP:0040284 - Very rare | | | 51 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NRIP1 CL E G H | 8204 | 8001 | OMIM:618270 | Congenital anomalies of kidney and urinary tract 3 | . | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | NSD1 CL E G H | 64324 | 14234 | ORPHA:821 | Sotos syndrome | HP:0040283 - Occasional | | | 544 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | OTUD5 CL E G H | 55593 | 25402 | OMIM:301056 | MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND | | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PAK2 CL E G H | 5062 | 8591 | ORPHA:1571 | Knobloch syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PAX2 CL E G H | 5076 | 8616 | OMIM:120330 | Papillorenal syndrome | . | | | 39 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PAX2 CL E G H | 5076 | 8616 | ORPHA:1475 | Renal coloboma syndrome | HP:0040282 - Frequent | | | 39 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PAX2 CL E G H | 5076 | 8616 | ORPHA:97362 | Renal hypoplasia, bilateral | | | | 39 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PAX6 CL E G H | 5080 | 8620 | OMIM:120200 | COLOBOMA, OCULAR, AUTOSOMAL DOMINANT | | | | 194 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PAX6 CL E G H | 5080 | 8620 | ORPHA:137902 | Isolated optic nerve hypoplasia/aplasia | HP:0040283 - Occasional | | | 194 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PBX1 CL E G H | 5087 | 8632 | OMIM:617641 | Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay | . | | | 3 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PBX1 CL E G H | 5087 | 8632 | ORPHA:97362 | Renal hypoplasia, bilateral | | | | 3 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PHC1 CL E G H | 1911 | 3182 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 16 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PIGA CL E G H | 5277 | 8957 | OMIM:300868 | Multiple congenital anomalies-hypotonia-seizures syndrome 2 | HP:0040283 - Occasional | | | 46 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PIGN CL E G H | 23556 | 8967 | ORPHA:2059 | Fryns syndrome | HP:0040283 - Occasional | | | 37 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PIGN CL E G H | 23556 | 8967 | OMIM:614080 | Multiple congenital anomalies-hypotonia-seizures syndrome 1 | HP:0040283 - Occasional | | | 37 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PIGO CL E G H | 84720 | 23215 | OMIM:614749 | Hyperphosphatasia with mental retardation syndrome 2 | | | | 84 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PIGQ CL E G H | 9091 | 14135 | OMIM:618548 | MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 4; MCAHS4 | | | | 3 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PLXNA1 CL E G H | 5361 | 9099 | OMIM:619955 | | | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | POLR3A CL E G H | 11128 | 30074 | ORPHA:3455 | Wiedemann-Rautenstrauch syndrome | HP:0040283 - Occasional | | | 138 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | POR CL E G H | 5447 | 9208 | ORPHA:95699 | Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency | HP:0040284 - Very rare | | | 76 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PPP3CA CL E G H | 5530 | 9314 | OMIM:618265 | Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development | . | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PRMT7 CL E G H | 54496 | 25557 | ORPHA:464288 | Short stature-brachydactyly-obesity-global developmental delay syndrome | HP:0040283 - Occasional | | | 6 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PSMD12 CL E G H | 5718 | 9557 | ORPHA:529962 | 17q24.2 microdeletion syndrome | HP:0040284 - Very rare | | | 4 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PUF60 CL E G H | 22827 | 17042 | ORPHA:508488 | 8q24.3 microdeletion syndrome | HP:0040283 - Occasional | | | 19 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | PYCR2 CL E G H | 29920 | 30262 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 11 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RAD21 CL E G H | 5885 | 9811 | ORPHA:199 | Cornelia de Lange syndrome | HP:0040282 - Frequent | | | 25 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RAD21 CL E G H | 5885 | 9811 | OMIM:611376 | Mungan syndrome | . | | | 25 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RALGAPA1 CL E G H | 253959 | 17770 | OMIM:618797 | NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION; NEDHRIT | | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RARB CL E G H | 5915 | 9865 | ORPHA:2470 | Matthew-Wood syndrome | HP:0040283 - Occasional | | | 9 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RBCK1 CL E G H | 10616 | 15864 | OMIM:615895 | Polyglucosan body myopathy 1 with or without immunodeficiency | | | | 10 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RBM8A CL E G H | 9939 | 9905 | OMIM:274000 | Thrombocytopenia-absent radius syndrome | | | | 10 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RECQL4 CL E G H | 9401 | 9949 | ORPHA:1225 | Baller-Gerold syndrome | HP:0040283 - Occasional | | | 445 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RERE CL E G H | 473 | 9965 | OMIM:616975 | Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart | | | | 16 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RERE CL E G H | 473 | 9965 | ORPHA:494344 | RERE-related neurodevelopmental syndrome | HP:0040283 - Occasional | | | 16 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RFC2 CL E G H | 5982 | 9970 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ROBO2 CL E G H | 6092 | 10250 | OMIM:610878 | VESICOURETERAL REFLUX 2; VUR2 | | | | 120 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RPL11 CL E G H | 6135 | 10301 | OMIM:612562 | Diamond-Blackfan anemia 7 | | | | 22 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | RREB1 CL E G H | 6239 | 10449 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SALL1 CL E G H | 6299 | 10524 | ORPHA:857 | Townes-Brocks syndrome | HP:0040283 - Occasional | | | 124 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SALL1 CL E G H | 6299 | 10524 | OMIM:107480 | Townes-Brocks syndrome 1 | . | | | 124 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SALL4 CL E G H | 57167 | 15924 | ORPHA:959 | Acro-renal-ocular syndrome | HP:0040283 - Occasional | | | 86 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SALL4 CL E G H | 57167 | 15924 | OMIM:607323 | Duane-Radial ray syndrome | . | | | 86 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SASS6 CL E G H | 163786 | 25403 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 4 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SDHA CL E G H | 6389 | 10680 | ORPHA:3208 | Isolated succinate-CoQ reductase deficiency | HP:0040284 - Very rare | | | 304 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SDHAF1 CL E G H | 644096 | 33867 | ORPHA:3208 | Isolated succinate-CoQ reductase deficiency | HP:0040284 - Very rare | | | 16 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SDHB CL E G H | 6390 | 10681 | ORPHA:3208 | Isolated succinate-CoQ reductase deficiency | HP:0040284 - Very rare | | | 237 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SDHD CL E G H | 6392 | 10683 | ORPHA:3208 | Isolated succinate-CoQ reductase deficiency | HP:0040284 - Very rare | | | 129 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SEC24C CL E G H | 9632 | 10705 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SEMA3E CL E G H | 9723 | 10727 | ORPHA:138 | CHARGE syndrome | HP:0040283 - Occasional | | | 16 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SETD2 CL E G H | 29072 | 18420 | ORPHA:821 | Sotos syndrome | HP:0040283 - Occasional | | | 60 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SF3B2 CL E G H | 10992 | 10769 | OMIM:164210 | Hemifacial microsomia | . | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SH2B1 CL E G H | 25970 | 30417 | ORPHA:261222 | Distal 16p11.2 microdeletion syndrome | HP:0040282 - Frequent | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SHANK3 CL E G H | 85358 | 14294 | ORPHA:48652 | Monosomy 22q13.3 | HP:0040283 - Occasional | | | 53 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SHANK3 CL E G H | 85358 | 14294 | OMIM:606232 | Phelan-Mcdermid syndrome | | | | 53 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SIX1 CL E G H | 6495 | 10887 | ORPHA:107 | BOR syndrome | HP:0040283 - Occasional | | | 50 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SIX1 CL E G H | 6495 | 10887 | OMIM:113650 | Branchiootorenal syndrome 1 | . | | | 50 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SIX1 CL E G H | 6495 | 10887 | OMIM:605192 | Deafness, autosomal dominant 23 | . | | | 50 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SIX5 CL E G H | 147912 | 10891 | ORPHA:107 | BOR syndrome | HP:0040283 - Occasional | | | 10 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SMC1A CL E G H | 8243 | 11111 | ORPHA:199 | Cornelia de Lange syndrome | HP:0040282 - Frequent | | | 135 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SMC3 CL E G H | 9126 | 2468 | ORPHA:199 | Cornelia de Lange syndrome | HP:0040282 - Frequent | | | 91 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SOX17 CL E G H | 64321 | 18122 | OMIM:613674 | Vesicoureteral reflux 3 | . | | | 3 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | SPOP CL E G H | 8405 | 11254 | OMIM:618828 | NABAIS SA-DE VRIES SYNDROME, TYPE 1; NSDVS1 | | | | 16 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | STAMBP CL E G H | 10617 | 16950 | OMIM:614261 | Microcephaly-Capillary malformation syndrome | HP:0040283 - Occasional | | | 24 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | STIL CL E G H | 6491 | 10879 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 99 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | STRA6 CL E G H | 64220 | 30650 | ORPHA:2470 | Matthew-Wood syndrome | HP:0040283 - Occasional | | | 71 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | STX1A CL E G H | 6804 | 11433 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TAF13 CL E G H | 6884 | 11546 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TBL2 CL E G H | 26608 | 11586 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TBX1 CL E G H | 6899 | 11592 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | 32 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TMEM270 CL E G H | 135886 | 23018 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TNXB CL E G H | 7148 | 11976 | OMIM:606408 | Ehlers-Danlos syndrome, classic-like | . | | | 134 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TNXB CL E G H | 7148 | 11976 | OMIM:615963 | Vesicoureteral reflux 8 | . | | | 134 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TP63 CL E G H | 8626 | 15979 | ORPHA:93930 | Bladder exstrophy | HP:0040281 - Very frequent | | | 140 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TP63 CL E G H | 8626 | 15979 | OMIM:604292 | Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 | . | | | 140 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TP63 CL E G H | 8626 | 15979 | ORPHA:1896 | EEC syndrome | HP:0040283 - Occasional | | | 140 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TRAPPC10 CL E G H | 7109 | 11868 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 1 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TRAPPC14 CL E G H | 55262 | 25604 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TRPS1 CL E G H | 7227 | 12340 | ORPHA:502 | Trichorhinophalangeal syndrome type 2 | HP:0040283 - Occasional | | | 171 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | TRRAP CL E G H | 8295 | 12347 | OMIM:618454 | Developmental delay with or without dysmorphic facies and autism | . | | | 2 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | UBE2A CL E G H | 7319 | 12472 | ORPHA:163956 | X-linked intellectual disability, Nascimento type | HP:0040282 - Frequent | | | 7 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | UFD1 CL E G H | 7353 | 12520 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | UNC45A CL E G H | 55898 | 30594 | OMIM:619377 | OSTEOOTOHEPATOENTERIC SYNDROME; OOHE | | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | VANGL1 CL E G H | 81839 | 15512 | ORPHA:3027 | Caudal regression sequence | HP:0040282 - Frequent | | | 111 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | VPS37D CL E G H | 155382 | 18287 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | WDR62 CL E G H | 284403 | 24502 | ORPHA:2512 | Autosomal recessive primary microcephaly | HP:0040282 - Frequent | | | 224 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ZEB2 CL E G H | 9839 | 14881 | ORPHA:261552 | Mowat-Wilson syndrome due to a ZEB2 point mutation | HP:0040283 - Occasional | | | 362 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ZEB2 CL E G H | 9839 | 14881 | ORPHA:261537 | Mowat-Wilson syndrome due to monosomy 2q22 | HP:0040283 - Occasional | | | 362 | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ZMIZ1 CL E G H | 57178 | 16493 | OMIM:618659 | NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA | | | | | | |
HP:0000076 | HP:0000076 | Vesicoureteral reflux | 0 | ZMYM2 CL E G H | 7750 | 12989 | OMIM:619522 | NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES; NECRC | | | | | | |
HP:0000076 | HP:0033739 | Secondary vesicoureteral reflux | 1 | CL E G H | | | | | | | | | | |
HP:0000076 | HP:0033738 | Primary vesicoureteral reflux | 1 | CL E G H | | | | | | | | | | |
HP:0000076 | HP:0033733 | Low-grade vesicoureteral reflux | 1 | UNC45A CL E G H | 55898 | 30594 | OMIM:619377 | OSTEOOTOHEPATOENTERIC SYNDROME; OOHE | | | | | | |
HP:0000076 | HP:0033734 | High-grade vesicoureteral reflux | 1 | ZMYM2 CL E G H | 7750 | 12989 | OMIM:619522 | NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES; NECRC | | | | | | |
HP:0000076 | HP:0033742 | Intrarenal reflux | 2 | CL E G H | | | | | | | | | | |
HP:0000076 | HP:0033741 | Grade IV vesicoureteral reflux | 2 | CL E G H | | | | | | | | | | |
HP:0000076 | HP:0033740 | Grade V vesicoureteral reflux | 2 | CL E G H | | | | | | | | | | |
HP:0000076 | HP:0033735 | Grade I vesicoureteral reflux | 2 | CL E G H | | | | | | | | | | |
HP:0000076 | HP:0033736 | Grade II vesicoureteral reflux | 2 | UNC45A CL E G H | 55898 | 30594 | OMIM:619377 | OSTEOOTOHEPATOENTERIC SYNDROME; OOHE | | | | | | |
HP:0000076 | HP:0033737 | Grade III vesicoureteral reflux | 2 | ZMYM2 CL E G H | 7750 | 12989 | OMIM:619522 | NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES; NECRC | | | | | | |