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Familial multinodular goiter

Disease Export to PDF
Name:
Familial multinodular goiter
Description:
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.
ORPHAcode:
276399
Synonyms:
FMNG
Familial MNG
Familial multinodular goiter syndrome
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
KEAP1
DICER1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14