multiple endocrine neoplasia type 1

Summary
Synonym
  • MEN type I
  • Wermer syndrome
  • Wermer's syndrome
Definition
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.
Super Class
autosomal dominant disease multiple endocrine neoplasia
External Links
Disease Ontology
DOID:10017
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 22 in total
Gene ID Gene Symbol Description Source
5728 PTEN phosphatase and tensin homolog
5837 PYGM glycogen phosphorylase, muscle associated
5973 RENBP renin binding protein
6389 SDHA succinate dehydrogenase complex flavoprotein subunit A
6390 SDHB succinate dehydrogenase complex iron sulfur subunit B
6391 SDHC succinate dehydrogenase complex subunit C
6392 SDHD succinate dehydrogenase complex subunit D
6652 SORD sorbitol dehydrogenase
6783 SULT1E1 sulfotransferase family 1E member 1
23583 SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024