loading...| Preferred Name |
Rhabdomyosarcoma |
|
| Synonyms |
|
|
| Definitions |
A malignant soft tissue tumor which develops from cells of striated muscle. It is the most common form of tumor found in children and adolescents. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_780 |
|
| definition |
A malignant soft tissue tumor which develops from cells of striated muscle. It is the most common form of tumor found in children and adolescents. |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=780 |
|
| has_age_of_onset |
Childhood |
|
| has_inheritance |
Multigenic/multifactorial |
|
| hasDbXref |
MedDRA:10039022 OMIM:268220 ICD-10:C49.9 ICD-11:2B55.1 ICD-11:2B55.Y ICD-11:2B55.2 ICD-11:2B55.0 UMLS:C0035412 OMIM:268210 ICD-11:2B55 MeSH:D012208 |
|
| label |
Rhabdomyosarcoma |
|
| notation |
ORPHA:780 |
|
| part_of | ||
| prefixIRI |
ORDO:Orphanet_780 |
|
| prefLabel |
Rhabdomyosarcoma |
|
| present_in |
Europe AND has_annual_incidence_average_value : 0.59 AND has_annual_incidence_range : 1-9 / 1 000 000 Worldwide AND has_point_prevalence_range : Unknown |
|
| treeView | ||
| subClassOf |