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congenital nongoitrous hypothyroidism 3 (CHNG3) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

congenital nongoitrous hypothyroidism 3

MONDO:0012360

Also known as:CHNG3hypothyroidism, congenital, nongoitrous, 3resistance to thyrotropin

Find Clinical TrialsTrials

Overview

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.

Clinical Trials1 registered · 1 recruiting

ResearchLimited published research (8 articles)

Diagnosis

Biomarker and diagnostic research for congenital nongoitrous hypothyroidism 3 has been reported in the published literature.

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

1 clinical trial registered, 1 recruiting. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.

8 publications have been identified in PubMed for congenital nongoitrous hypothyroidism 3. Research spans Basic Science / Preclinical (63%), Diagnostic / Biomarker (13%), and Review / Meta-Analysis (13%).

Recent Publications

Hajali TA (2026). [PMID: 41684033](https://pubmed.ncbi.nlm.nih.gov/41684033/). *International journal of molecular sciences*. [Basic Science / Preclinical]
Korkmaz HA (2025). [PMID: 39857886](https://pubmed.ncbi.nlm.nih.gov/39857886/). *Children (Basel, Switzerland)*. [Basic Science / Preclinical]
Shima H (2025). [PMID: 40494332](https://pubmed.ncbi.nlm.nih.gov/40494332/). *Hormone research in paediatrics*. [Review / Meta-Analysis]
Fang L (2025). [PMID: 40908484](https://pubmed.ncbi.nlm.nih.gov/40908484/). *BMC endocrine disorders*. [Diagnostic / Biomarker]
Yalçın HY (2024). [PMID: 38841327](https://pubmed.ncbi.nlm.nih.gov/38841327/). *Molecular syndromology*. [Case Report / Case Series]

Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 10:51 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:609893

Questions for Your Care Team

→Are any of the 1 active clinical trial a good fit for my situation?
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congenital nongoitrous hypothyroidism 3

Overview

Diagnosis

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

Related Diseases

Questions for Your Care Team

Questions for Your Care Team