Overview
Familial dysalbuminaemic hyperthyroxinaemia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Asymptomatic hyperthyroxinemia
Always present (100%)HP:0008247
Increased circulating free T4 concentration
Always present (100%)HP:0033077
Abnormal circulating free T4 concentration
Excluded (<1%)HP:0033076
Abnormal thyrotropin level
Excluded (<1%)HP:0031097
Quick Facts
- SNOMED CT
- 237547004
- UMLS CUI
- C0342185
- Fully Specified Name
- Familial dysalbuminemic hyperthyroxinemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 4
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.