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thyroid dyshormonogenesis 5

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the DUOXA2 gene.
Uniprot Description A disorder due to thyroid dyshormonogenesis, causing hypothyroidism, goiter, and variable mental deficits derived from unrecognized and untreated hypothyroidism.
Mondo Term and Equivalent IDs
MONDO:0010137:  thyroid dyshormonogenesis 5
MESH:C562771: 
SCTID:63127008: 
UMLS:C0342196: