MeSH Browser

MeSH Supplementary: Euthyroid Goiter
Unique ID: C562732
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562732
Entry Term(s): Goiter, multinodular 1, with or without sertoli-leydig cell tumors; Goiter, nontoxic, with intrathyroidal calcification; Multinodular goiter, adolescent; Simple goiter
Registry Numbers: 0
Heading Mapped to: *Goiter, Nodular
Frequency: 143
Note: 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
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Euthyroid Goiter MeSH Supplementary Concept Data 2025