Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare thyroid disease characterized by familial occurrence of thyroid enlargement due to the development of multiple hyperplastic nodules with onset in childhood or adolescence. The condition is commonly associated with the development of other benign or malignant tumors. Disease data Classification Disease Synonyms FMNG FMNG Rodzinne MNG Familial MNG Familial multinodular goiter syndrome ORPHA code 276399 OMIM code 138800 ICD10 code E04.2 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl