Also known as MEN1, Multiple Endocrine Adenomatosis, MEN type I, Wermer syndrome, Wermer's syndrome, Mea 1, Multiple Endocrine Neoplasia Type 1, MEN1 syndrome
via PubMed
autosomal dominant disease 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
via Wikidata · CC0
via Wikidata sitelinks · CC0
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).