loading...| Preferred Name |
Hypereosinophilic syndrome |
|
| Synonyms |
HES |
|
| Definitions |
Hypereosinophilic syndrome (HES) constitutes a rare and heterogeneous group of disorders, defined as persistent and marked blood eosinophilia and/or tissue eosinophilia associated with a wide range of clinical manifestations reflecting eosinophil-induced tissue/organ damage. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_168956 |
|
| alternative_term |
HES |
|
| definition |
Hypereosinophilic syndrome (HES) constitutes a rare and heterogeneous group of disorders, defined as persistent and marked blood eosinophilia and/or tissue eosinophilia associated with a wide range of clinical manifestations reflecting eosinophil-induced tissue/organ damage. |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=168956 |
|
| has_age_of_onset |
All ages |
|
| has_inheritance |
Not applicable Unknown |
|
| hasDbXref |
UMLS:C1540912 MedDRA:10048643 MeSH:D017681 |
|
| label |
Hypereosinophilic syndrome |
|
| notation |
ORPHA:168956 Clinical group |
|
| prefixIRI |
ORDO:Orphanet_168956 |
|
| prefLabel |
Hypereosinophilic syndrome |
|
| present_in |
United States AND has_point_prevalence_average_value : 3.3 AND has_point_prevalence_range : 1-9 / 100 000 Europe AND has_point_prevalence_range : Unknown Europe AND has_annual_incidence_range : <1 / 1 000 000 United States AND has_annual_incidence_average_value : 0.027 AND has_annual_incidence_range : <1 / 1 000 000 |
|
| subClassOf |
http://www.orpha.net/ORDO/Orphanet_557492 |