Multiple endocrine neoplasia

rare

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.

Identifiers: MONDO:0017169 Orphanet:276161
Part of: Hereditary neoplastic syndrome Multiple polyglandular tumor Neurocristopathy
Also known as: MEN · men syndrome · men syndromes · multiple endocrine adenomatosis · multiple endocrine neoplasia syndrome

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Multiple endocrine neoplasia type 2	MONDO:0019003	3
Multiple endocrine neoplasia type 1	MONDO:0007540		MEN1
Multiple endocrine neoplasia type 4	MONDO:0012552		CDKN1B

Rare disease

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