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thyroid dyshormonogenesis 6

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOX2 gene.
Uniprot Description A disorder due to a defective conversion of accumulated iodide to organically bound iodine. The iodide organification defect can be partial or complete.
Mondo Term and Equivalent IDs
MONDO:0011792:  thyroid dyshormonogenesis 6
MESH:C564608: 
UMLS:C1846632: