Alveolar rhabdomyosarcoma
General Information (adopted from Orphanet):
| Synonyms, Signs: |
RHABDOMYOSARCOMA, ALVEOLAR RMSA RMS2 |
| Number of Symptoms | 2 |
| OrphanetNr: | 99756 |
| OMIM Id: |
268220
|
| ICD-10: |
C49 |
| UMLs: |
C0206655 |
| MeSH: |
D018232 |
| MedDRA: |
10065867 |
| Snomed: |
404053004 63449009 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal recessive inheritance [Omim] |
| Age of onset: |
|
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Rhabdomyosarcoma
-Rare neurologic disease -Rare oncologic disease |
Symptom Information:
|
|
(HPO:0006779) | Alveolar rhabdomyosarcoma | 1 / 7739 | ||||
|
|
(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|