ORPHA:276161
Multiple endocrine neoplasia
Synonyms: MEN
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Autosomal dominant, Not applicable
- Age of onset
- All ages
- Status
- active
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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Multiple endocrine neoplasia | MEN |
| fr | Néoplasie endocrinienne multiple | = en |
| de | Neoplasie, endokrine multiple | = en |
| es | Neoplasia endocrina múltiple | = en |
| it | Neoplasia endocrina multipla | = en |
| nl | Multipele endocriene neoplasie | MEN · Meervoudige endocriene neoplasie |
| pt | Neoplasia endócrina múltipla | |
| pl | Zespół mnogiej gruczolakowatości wewnątrzwydzielniczej | = en |
| cs | Mnohočetná endokrinní neoplázie | = en |
| uk | Множинні ендокринні неоплазії | = en |
| zh | 多发性内分泌肿瘤 | = en |
| tr | Çoklu endokrin neoplazi | = en |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D44.8 | E | specific | validated |
| ICD-11 | 2F7A.Y | NTBT | index | validated |
| MONDO | 0017169 | E | validated | |
| MONDO | 17169 | E | validated | |
| MeSH | D009377 | E | validated | |
| UMLS | C0027662 | E | validated | |
| MedDRA | 10028196 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:100094Multiple polyglandular tumor
rare genetic diseases; rare endocrine diseases; rare neoplastic diseases
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | 0.05 / 100 000 | Ireland | Value and class | Validated | 2575263[PMID] |
| Point prevalence | Unknown | — | Europe | Class only | Validated | ORPHANET_[EXPERT] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/276161
- This record as JSON: /data/d/276161.json