Congenital nongoitrous hypothyroidism 3

MONDO:0012360

A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1.

Also known as: CHNG3, hypothyroidism, congenital, nongoitrous, 3, resistance to thyrotropin, thyrotropin resistance

1 clinical trial for this condition and its sub-types, 0 tagged with Congenital nongoitrous hypothyroidism 3 itself.

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Where it sits in the disease tree

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Part of

↑ Hypothyroidism, congenital, nongoitrous (1) ↑ Peripheral resistance to thyroid hormones (0)

Including sub-types (1) Tagged with Congenital nongoitrous hypothyroidism 3 (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

Congenital nongoitrous hypothyroidism 3

Where it sits in the disease tree

Scientists watch thyroid conditions unfold in 2,500 patients