Pendred syndrome

MONDO:0010134

Pendred syndrome (PDS) is a clinically variable genetic disorder characterized by bilateral sensorineural hearing loss and euthyroid goiter.

Also known as: Pendred syndrome, TDH2B, deafness with goiter, deafness with goitre, goiter-deafness syndrome, hypothyroidism, congenital, due to dyshormonogenesis, 2B, thyroid dyshormonogenesis 2B, thyroid hormonogenesis, genetic defect in, 2B

1 clinical trial for this condition and its sub-types, 0 tagged with Pendred syndrome itself.

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Where it sits in the disease tree

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↑ Syndromic disease (7133) ↑ Autosomal recessive disease (994) ↑ Congenital hypothyroidism (14)

Including sub-types (1) Tagged with Pendred syndrome (0)

Trials to join now! 1

Scientists watch thyroid conditions unfold in 2,500 patients

Knowledge-focused Recruiting now

This study follows up to 2,500 people with thyroid problems like hyperthyroidism, hypothyroidism, or Graves' disease. Researchers will track how these conditions develop over time using standard medical tests and genetic samples. The goal is to better understand the natural histo…

Sponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) • Aim: Knowledge-focused

Last updated Sep 18, 2026 00:00 UTC

Pendred syndrome

Where it sits in the disease tree

Scientists watch thyroid conditions unfold in 2,500 patients