loading...| Preferred Name | Langerhans cell histiocytosis | |
| Synonyms |
Histiocytosis X Langerhans cell granulomatosis |
|
| Definitions |
A rare systemic disease characterized by the accumulation (usually organized in granulomas) of macrophage, bearing the features of Langerhans cells in various tissues. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_389 |
|
| alternative_term |
Histiocytosis X Langerhans cell granulomatosis |
|
| definition |
A rare systemic disease characterized by the accumulation (usually organized in granulomas) of macrophage, bearing the features of Langerhans cells in various tissues. |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=389 |
|
| has_age_of_onset |
All ages |
|
| has_inheritance |
Unknown |
|
| hasDbXref |
OMIM:604856 ICD-10:C96.6 MedDRA:10069698 UMLS:C0019621 ICD-11:2B31.2Y ICD-11:2B31.20 ICD-10:C96.0 ICD-11:2B31.2 ICD-10:C96.5 MeSH:D006646 |
|
| label |
Langerhans cell histiocytosis |
|
| notation |
ORPHA:389 |
|
| part_of |
http://www.orpha.net/ORDO/Orphanet_506210 http://www.orpha.net/ORDO/Orphanet_182222 |
|
| prefixIRI |
ORDO:Orphanet_389 |
|
| prefLabel |
Langerhans cell histiocytosis |
|
| present_in |
Europe AND has_point_prevalence_average_value : 1.5 AND has_point_prevalence_range : 1-9 / 100 000 |
|
| treeView |
http://www.orpha.net/ORDO/Orphanet_506210 http://www.orpha.net/ORDO/Orphanet_182222 |
|
| subClassOf |