Gilbert's syndrome

disorder

SNOMED 27503000CUI C0017551

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Unconjugated hyperbilirubinemia

Always present (100%)HP:0008282

Elevated liver enzymes

Excluded (<1%)HP:0002910

Hepatic insufficiency

Excluded (<1%)HP:0001399

Yellowing of the skin

HP:0000952

Related Conditions

Inherited disorder of bilirubin metabolism(parent)

Quick Facts

SNOMED CT: 27503000
UMLS CUI: C0017551
Fully Specified Name: Gilbert's syndrome (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.