DISEASES

Disease-gene associations mined from literature

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Human genes for multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 1 [DOID:10017]

A multiple endocrine neoplasia that has_material_basis_in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas.

Synonyms:  multiple endocrine neoplasia type 1,  DOID:10017,  MEN type I,  Wermer's syndrome,  Wermer syndrome ...

Linkouts:  OMIM

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.