Congenital hydronephrosis
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 6 |
| OrphanetNr: | 2190 |
| OMIM Id: |
|
| ICD-10: |
Q62.0 |
| UMLs: |
C0266316 |
| MeSH: |
|
| MedDRA: |
10050975 |
| Snomed: |
16297002 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant [Orphanet] |
| Age of onset: |
Neonatal [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Genetic nonsyndromic renal or urinary tract malformation
-Rare genetic disease Nonsyndromic renal or urinary tract malformation -Rare developmental defect during embryogenesis -Rare renal disease |
Symptom Information:
|
|
(HPO:0000072) | Hydroureter | Very frequent [Orphanet] | 146 / 7739 | |||
|
|
(HPO:0000069) | Abnormality of the ureter | Frequent [Orphanet] | 47 / 7739 | |||
|
|
(HPO:0000079) | Abnormality of the urinary system | Occasional [Orphanet] | 88 / 7739 | |||
|
|
(HPO:0001561) | Polyhydramnios | Occasional [Orphanet] | 191 / 7739 | |||
|
|
(HPO:0001562) | Oligohydramnios | Occasional [Orphanet] | 75 / 7739 | |||
|
|
(HPO:0001626) | Abnormality of the cardiovascular system | Occasional [Orphanet] | 73 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|