Familial vesicoureteral reflux
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Familial VUR |
| Number of Symptoms | 2 |
| OrphanetNr: | 289365 |
| OMIM Id: |
193000
610878 613674 614317 614318 614319 615390 |
| ICD-10: |
N13.7 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant [Orphanet] |
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Genetic urogenital tract malformation
-Rare genetic disease Nonsyndromic urogenital tract malformation of male and female -Rare developmental defect during embryogenesis -Rare urogenital disease |
Symptom Information:
|
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(HPO:0000076) | Vesicoureteral reflux | 94 / 7739 | ||||
|
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(HPO:0000924) | Abnormality of the skeletal system | 114 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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