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loading...| Preferred Name |
Multiple endocrine neoplasia |
| 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-10:D44.8 ICD-11:2F7A.0 UMLS:C0027662 MedDRA:10061299 |
| label |
Multiple endocrine neoplasia |
| notation |
Clinical group ORPHA:276161 |
| prefixIRI |
ORDO:Orphanet_276161 |
| prefLabel |
Multiple endocrine neoplasia |
| present_in |
Ireland AND has_annual_incidence_average_value : 0.05 AND has_annual_incidence_range : <1 / 1 000 000 Europe AND has_point_prevalence_range : Unknown |
| subClassOf |
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