Ureteropelvic junction obstruction
Symptom Information:
Symptom ID: | HPO:0000074 | ||||||||||
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) Ureteral obstruction(HPO:0006000) Ureteral stenosis(HPO:0000071) Ureteropelvic junction obstruction(HPO:0000074) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal obstructive disorders(MedDRA:10038488) Ureteropelvic junction obstruction(HPO:0000074) |
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Database Frequency: | 15 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Bilateral multicystic renal dysplasia | (Orphanet:97364) |
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO | (OMIM:610805) |
DUAL SERINE/THREONINE AND TYROSINE PROTEIN KINASE | (OMIM:612666) |
Goldenhar syndrome | (Orphanet:374) |
Hand-foot-genital syndrome | (Orphanet:2438) |
KABUKI SYNDROME 1 | (OMIM:147920) |
Kabuki syndrome | (Orphanet:2322) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Multicystic renal dysplasia | (Orphanet:1851) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Steinert myotonic dystrophy | (Orphanet:273) |
VACTERL/VATER association | (Orphanet:887) |
Zunich-Kaye syndrome | (Orphanet:3474) |