Familial thyroid dyshormonogenesis

MONDO:0010132

A type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis.

Also known as: dyshormonogenesis, nongoitrous hyperthyrotropinemia, thyroid dyshormonogenesis

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

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by