All diseases

OMIM ID
131100
OMIM term:
MULTIPLE ENDOCRINE NEOPLASIA, TYPE I; MEN1
Alternative terms:
MEN I
ENDOCRINE ADENOMATOSIS, MULTIPLE
MEA I
WERMER SYNDROME MEN1 SOMATIC MUTATIONS, INCLUDED
(∗) Location:
11q13.1  
(†) Associated OMIM genes:
MEN1  
(‡) Associated MGI genes:
Men1  

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