Abnormality of the ureter
Symptom Information:
Symptom ID: | HPO:0000069 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) 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) MedDRA: |
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Database Frequency: | 47 / 7739 | |||
Resource: |
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) |