Clinical Trials
1
Total Trials
0
Recruiting
0
With Results
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Congenital goitre
HP:0008251
Congenital hypothyroidism
HP:0000851
Hearing impairment
HP:0000365
Laboratory abnormality
HP:0001939
Nonprogressive mental retardation
HP:0001249
Spastic diparesis
HP:0001264
Related Conditions
Congenital hypothyroidism without goitre(child)
Goitrous cretin(child)
Myxedematous form of cretinism(child)
Endemic cretinism(child)
Sporadic cretinism(child)
Multiple malformation syndrome due to non-infectious environmental agents(parent)
Iodine deficiency syndrome(parent)
Congenital anomaly of the thyroid gland(parent)
Quick Facts
- SNOMED CT
- 217710005
- UMLS CUI
- C3165526
- Fully Specified Name
- Congenital iodine deficiency syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 6
- 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.