Familial prostate cancer
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 2 |
| OrphanetNr: | 1331 |
| OMIM Id: |
176807
300147 300704 601518 602759 603688 608656 608658 609299 609558 610321 610997 611100 611868 611928 611955 611958 611959 614731 |
| ICD-10: |
C61 |
| UMLs: |
C2931456 |
| MeSH: |
C537243 |
| MedDRA: |
|
| Snomed: |
|
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
|
| Age of onset: |
Adult [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Genetic urogenital tumor
-Rare genetic disease Rare genetic urogenital disease -Rare genetic disease Rare urinary tract tumor -Rare oncologic disease -Rare urogenital disease |
Symptom Information:
|
|
(HPO:0012125) | Prostate cancer | 6 / 7739 | ||||
|
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|