Abnormality of the ureter

Symptom Information:

Symptom ID: HPO:0000069
Abnormality of the ureters [HPO:0000069]
Ureteral anomalies [HPO:0000069]
Ureteral anomalies [OMIM:Ureteral anomalies]
Cross references:
OMIM: "Ureteral anomalies" [OMIM:Ureteral anomalies]
Is a (Direct Parents):
HPO         Abnormality of the upper urinary tract
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the ureter(HPO:0000069)
Database Frequency: 47 / 7739

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acro-renal-mandibular syndrome (Orphanet:958)
Alagille syndrome (Orphanet:52)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal recessive spondylocostal dysostosis (Orphanet:2311)
Baller-Gerold syndrome (Orphanet:1225)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 (Orphanet:231117)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)
Caudal duplication (Orphanet:1756)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Cleft palate - short stature - vertebral anomalies (Orphanet:2015)
Congenital hydronephrosis (Orphanet:2190)
Corpus callosum agenesis - double urinary collecting system (Orphanet:1492)
Diabetic embryopathy (Orphanet:1926)
Distal monosomy 13q (Orphanet:1590)
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria (Orphanet:1035)
Familial caudal dysgenesis (Orphanet:1768)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Hand-foot-genital syndrome (Orphanet:2438)
Hirschsprung disease - nail hypoplasia - dysmorphism (Orphanet:2153)
Humero-radio-ulnar synostosis (Orphanet:3266)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Knobloch syndrome (Orphanet:1571)
Koolen-De Vries syndrome (Orphanet:96169)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
Lower limb deficiency - hypospadias (Orphanet:2487)
Meckel syndrome (Orphanet:564)
Microcephaly - cervical spine fusion anomalies (Orphanet:2522)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Opitz G/BBB syndrome (Orphanet:2745)
Penoscrotal transposition (Orphanet:2842)
Peters-plus syndrome (Orphanet:709)
Peutz-Jeghers syndrome (Orphanet:2869)
Premature chromosome condensation with microcephaly and intellectual deficit (Orphanet:52183)
Renal caliceal diverticuli - deafness (Orphanet:2838)
Ring chromosome 8 (Orphanet:1450)
Scalp-ear-nipple syndrome (Orphanet:2036)
Silver-Russell syndrome (Orphanet:813)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Sotos syndrome (Orphanet:821)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Trisomy 13 (Orphanet:3378)
Trisomy 20p (Orphanet:261318)
Urban-Rogers-Meyer syndrome (Orphanet:3409)