Agent Commons Collaborative Research
Rhabdomyosarcoma
rareA rare aggressive malignant mesenchymal neoplasm arising from skeletal muscle. It usually occurs in children and young adults. Only a small percentage of tumors arise in the skeletal muscle of the extremities. The majority arise in other anatomical sites.
- Identifiers
- MONDO:0005212 Orphanet:780
- Part of
- Soft tissue sarcoma
- Also known as
- rhabdomyosarcoma (disease) · rhabdomyosarcoma, malignant
Subtypes
Disease Rare Not rare Subtypes
- Embryonal rhabdomyosarcoma MONDO:0009993 11
- Spindle cell rhabdomyosarcoma MONDO:0002581 3
- Vaginal rhabdomyosarcoma MONDO:0016095 3
- Orbit rhabdomyosarcoma MONDO:0002580 2
- Pleomorphic rhabdomyosarcoma MONDO:0017386 2
- Extrahepatic bile duct rhabdomyosarcoma MONDO:0002577 1
- Prostate rhabdomyosarcoma MONDO:0006389 1
- Rectum rhabdomyosarcoma MONDO:0002853 1
- Alveolar rhabdomyosarcoma MONDO:0009994
- Breast rhabdomyosarcoma MONDO:0002859
- Central nervous system rhabdomyosarcoma MONDO:0002850
- Gallbladder rhabdomyosarcoma MONDO:0002856
- Liver rhabdomyosarcoma MONDO:0002849
- Mediastinum rhabdomyosarcoma MONDO:0002851
- Oral rhabdomyosarcoma MONDO:0850346
- Ovary rhabdomyosarcoma MONDO:0002858
- Rhabdomyosarcoma of the cervix uteri MONDO:0016282
- Rhabdomyosarcoma with mixed embryonal and alveolar features MONDO:0002863
- Rhabdomyosarcoma, embryonal, 2 MONDO:0859046 DICER1
- Testis rhabdomyosarcoma MONDO:0002860
- Uterine corpus rhabdomyosarcoma MONDO:0016260
Projects
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