loading...| Preferred Name | Multiple endocrine neoplasia | |
| Synonyms |
MEN |
|
| Definitions |
Multiple endocrine neoplasia (MEN) is a group of rare inherited cancer syndromes characterized by the development of two or more endocrine gland tumors, sometimes with tumor development in other tissues or organs. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_276161 |
|
| alternative_term |
MEN |
|
| definition |
Multiple endocrine neoplasia (MEN) is a group of rare inherited cancer syndromes characterized by the development of two or more endocrine gland tumors, sometimes with tumor development in other tissues or organs. |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=276161 |
|
| has_age_of_onset |
All ages |
|
| has_inheritance |
Not applicable Autosomal dominant |
|
| hasDbXref |
ICD-11:2F7A.Y MeSH:D009377 ICD-10:D44.8 MedDRA:10061299 UMLS:C0027662 |
|
| label |
Multiple endocrine neoplasia |
|
| notation |
ORPHA:276161 Clinical group |
|
| prefixIRI |
ORDO:Orphanet_276161 |
|
| prefLabel |
Multiple endocrine neoplasia |
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| present_in |
Europe AND has_point_prevalence_range : Unknown Ireland AND has_annual_incidence_average_value : 0.05 AND has_annual_incidence_range : <1 / 1 000 000 |
|
| subClassOf |