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Orphanet Rare Disease Ontology
Last uploaded:
July 3, 2024
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| Preferred Name | Desmoid tumor | |
| Synonyms |
Aggressive fibromatosis Desmoid type fibromatosis |
|
| Definitions |
A desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_873 |
|
| alternative_term |
Aggressive fibromatosis Desmoid type fibromatosis
|
|
| definition |
A desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential.
|
|
| definition_citation |
Orphanet
|
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=873 |
|
| has_age_of_onset |
Adolescent Adult
|
|
| has_inheritance |
Not applicable Unknown
|
|
| hasDbXref |
OMIM:135290 UMLS:C0079218 ICD-10:D48.1
|
|
| label |
Desmoid tumor
|
|
| notation |
ORPHA:873
|
|
| part_of | ||
| prefixIRI |
ORDO:Orphanet_873
|
|
| prefLabel |
Desmoid tumor
|
|
| present_in |
Finland AND has_annual_incidence_average_value : 0.33 AND has_annual_incidence_range : 1-9 / 1 000 000 Europe AND has_annual_incidence_average_value : 0.3 AND has_annual_incidence_range : 1-9 / 1 000 000 Worldwide AND has_point_prevalence_range : Unknown
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| treeView | ||
| subClassOf |
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