Thyroid dyshormonogenesis 4

MONDO:0010136

Any familial thyroid dyshormonogenesis in which the cause of the disease is a mutation in the IYD gene.

Also known as: IYD familial thyroid dyshormonogenesis, TDH4, familial thyroid dyshormonogenesis caused by mutation in IYD, hypothyroidism, congenital, due to dyshormonogenesis, 4, thyroid dyshormonogenesis 4, thyroid dyshormonogenesis type 4, thyroid hormonogenesis, genetic defect in, 4, deiodinase deficiency

0 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.