Familial dysalbuminaemic hyperthyroxinaemia

disorder

SNOMED 237547004CUI C0342185

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

Related Conditions

Hyperthyroidism(parent)

Thyroid hormone binding abnormality(parent)

Familial disease(parent)

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.