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Euthyroid Goiter MeSH Supplementary Concept Data 2025
A common hereditary autosomal dominant disorder characterized by nodular enlargement of the THYROID GLAND. In MNG1, some individuals may also develop SERTOLI-LEYDIG CELL TUMORS, usually of the OVARY. Mutations in the DICER1 gene have been identified for MNG1. OMIM: 138800