Thyroid dyshormonogenesis 3

MONDO:0010135

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

Also known as: TDH3, TG familial thyroid dyshormonogenesis, familial thyroid dyshormonogenesis caused by mutation in TG, hypothyroidism, congenital, due to dyshormonogenesis, 3, thyroid dyshormonogenesis 3, thyroid dyshormonogenesis type 3, thyroid hormonogenesis, genetic defect in, 3

2 clinical trials for this condition and its sub-types, 1 tagged with Thyroid dyshormonogenesis 3 itself.

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Where it sits in the disease tree

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Part of

↑ Familial thyroid dyshormonogenesis (4)

Including sub-types (2) Tagged with Thyroid dyshormonogenesis 3 (1)

Not yet finished but already full! 1

Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC

Thyroid dyshormonogenesis 3

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth