Clinical Trials
1
Total Trials
0
Recruiting
0
With Results
Related Conditions
Congenital hypothyroidism without goitre(child)
Goitrous cretin(child)
Sporadic cretinism(child)
Iodide oxidation defect(child)
Iodide transport defect(child)
Hypothyroidism due to defect in thyroid hormone synthesis(child)
Myxedematous form of cretinism(child)
Athyrotic hypothyroidism sequence(child)
Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody(child)
Idiopathic congenital hypothyroidism(child)
Familial thyroid dyshormonogenesis(child)
Hypothyroidism due to mutation in transcription factor of pituitary development(child)
Congenital hypothyroidism due to absence of thyroid gland(child)
Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome(child)
Bamforth Lazarus syndrome(child)
Congenital central hypothyroidism(child)
Congenital hypothyroidism due to iodine deficiency(child)
Short stature with delayed bone age due to thyroid hormone metabolism deficiency(child)
Genetic transient congenital hypothyroidism(child)
Congenital hypothyroidism due to maternal intake of antithyroid drug(child)
Quick Facts
- SNOMED CT
- 190268003
- UMLS CUI
- C0010308
- Fully Specified Name
- Congenital hypothyroidism (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- Clinical Trials
- 1
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.