loading...| Preferred Name | Buerger disease | |
| Synonyms |
Thromboangiitis obliterans |
|
| Definitions |
A rare systemic disease characterized by inflammatory, non-necrotizing, non-atherosclerotic, occlusive vascular disease with thrombosis and recanalization affecting small and medium sized arteries and veins of upper and lower extremities. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_36258 |
|
| alternative_term |
Thromboangiitis obliterans |
|
| definition |
A rare systemic disease characterized by inflammatory, non-necrotizing, non-atherosclerotic, occlusive vascular disease with thrombosis and recanalization affecting small and medium sized arteries and veins of upper and lower extremities. |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=36258 |
|
| has_age_of_onset |
Adult |
|
| has_inheritance |
Not applicable |
|
| hasDbXref |
MedDRA:10043540 ICD-11:4A44.8 OMIM:211480 UMLS:C0040021 MeSH:D013919 ICD-10:I73.1 |
|
| label |
Buerger disease |
|
| notation |
ORPHA:36258 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_36258 |
|
| prefLabel |
Buerger disease |
|
| present_in |
Worldwide AND has_point_prevalence_average_value : 16.0 AND has_point_prevalence_range : 1-5 / 10 000 Europe AND has_point_prevalence_average_value : 10.0 AND has_point_prevalence_range : 1-5 / 10 000 |
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| treeView | ||
| subClassOf |