Inherited thyroid metabolism disease
MONDO:0045046An inherited metabolic disease that is has its basis in the disruption of thyroid hormone metabolic process.
Also known as: inborn error of thyroid hormone metabolic process, inborn thyroid hormone metabolic process disorder, inherited disorder of thyroid metabolism, rare inborn error of thyroid hormone metabolic process
8 clinical trials for this condition and its sub-types, 0 tagged with Inherited thyroid metabolism disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inherited thyroid metabolism disease
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Thyroid hormone resistance syndrome 3 trials · 4 incl. sub-types
4 sub-types
- Generalized resistance to thyroid hormone 1 trial · 2 incl. sub-types Sub-types →
- Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta 1 trial · 2 incl. sub-types Sub-types →
- Resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha 1 trial
- Selective peripheral resistance to thyroid hormone 0 trials
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Familial thyroid dyshormonogenesis 1 trial · 4 incl. sub-types
6 sub-types
- Thyroid dyshormonogenesis 2A 4 trials
- Thyroid dyshormonogenesis 1 1 trial
- Thyroid dyshormonogenesis 3 1 trial
- Thyroid dyshormonogenesis 5 1 trial
- Thyroid dyshormonogenesis 6 1 trial
- Thyroid dyshormonogenesis 4 0 trials
Most studied deeper sub-types
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New pill shows promise for fatty liver in major trial
Disease control OngoingThis study tests a daily pill called resmetirom in people with non-alcoholic fatty liver disease (NAFLD). The goal is to see if it safely reduces liver fat and cholesterol over 52 weeks. About 810 adults who completed earlier related studies are taking part. This is a long-term t…
Phase 3 • Sponsor: Madrigal Pharmaceuticals, Inc. • Aim: Disease control
Last updated Jun 27, 2026 12:38 UTC
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Newborn screening study aims to catch rare diseases at birth
Diagnosis OngoingThis 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