Central congenital hypothyroidism

MONDO:0016410

Central or secondary congenital hypothyroidism is a type of permanent congenital hypothyroidism characterized by permanent thyroid hormone deficiency that is present from birth and secondary to a disorder in the thyroid-stimulating hormone (TSH) - thyrotropin-releasing hormone (TRH) system.

Also known as: TSH deficiency, central hypothyroidism, hypothalamic-pituitary hypothyroidism, secondary hypothyroidism, thyroid stimulating hormone deficiency, thyrotropin deficiency

3 clinical trials for this condition and its sub-types, 1 tagged with Central congenital hypothyroidism itself.

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Where it sits in the disease tree

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↑ Permanent congenital hypothyroidism (3)

Sub-types of Central congenital hypothyroidism

Including sub-types (3) Tagged with Central congenital hypothyroidism (1)

Trials to join now! 2 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

Central congenital hypothyroidism

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth