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Orphanet Rare Disease Ontology
Last uploaded:
December 4, 2024
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| Id | http://www.orpha.net/ORDO/Orphanet_293202
http://www.orpha.net/ORDO/Orphanet_293202
|
|---|---|
| Preferred Name | Epithelioid sarcoma |
| Definitions |
A rare, soft tissue tumor characterized by high incidence of local recurrence, regional lymph node involvement and distant metastases. It commonly affects the soft tissue under the skin of a finger, hand, forearm, lower leg or foot, less often other areas of the body.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition_citation | Orphanet |
|---|---|
| definition | A rare, soft tissue tumor characterized by high incidence of local recurrence, regional lymph node involvement and distant metastases. It commonly affects the soft tissue under the skin of a finger, hand, forearm, lower leg or foot, less often other areas of the body. |
| label |
Epithelioid sarcoma
|
| prefLabel |
Epithelioid sarcoma
|
| hasDbXref |
UMLS:C0205944
ICD-10:C49.9
ICD-11:2B5F.2
MedDRA:10015099
ICD-11:XH4F96
|
| notation |
ORPHA:293202
|
| present_in |
United States AND has_annual_incidence_average_value : 0.04 AND has_annual_incidence_range : <1 / 1 000 000
Europe AND has_annual_incidence_range : <1 / 1 000 000
Europe AND has_point_prevalence_range : <1 / 1 000 000
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| part_of | |
| prefixIRI |
ORDO:Orphanet_293202
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| expertlink | |
| subClassOf | |
| type | |
| has_inheritance |
Not applicable
|
| has_age_of_onset |
Adolescent
Adult
Childhood
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