Rhabdomyosarcoma
General Information (adopted from Orphanet):
| Synonyms, Signs: |
|
| Number of Symptoms | 2 |
| OrphanetNr: | 780 |
| OMIM Id: |
268210
268220 |
| ICD-10: |
C49 |
| UMLs: |
C0035412 |
| MeSH: |
D012208 |
| MedDRA: |
10039022 |
| Snomed: |
302847003 30924005 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Multifactorial [Orphanet] |
| Age of onset: |
Childhood [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Muscular tumor
-Rare neurologic disease Soft tissue sarcoma -Rare oncologic disease |
Symptom Information:
|
|
(HPO:0006743) | Embryonal rhabdomyosarcoma | 3 / 7739 | ||||
|
|
(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|