Rotor syndrome

disorder

SNOMED 32891000CUI C0220991

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.

Abnormal circulating enzyme concentration or activity

Very frequent (80-99%)HP:0012379

Conjugated hyperbilirubinemia

Very frequent (80-99%)HP:0002908

Yellowing of the skin

Very frequent (80-99%)HP:0000952

Bilirubinuria

Frequent (30-79%)HP:0031811

High blood bilirubin levels

Frequent (30-79%)HP:0002904

Porphyrinuria

Frequent (30-79%)HP:0010473

Conjunctival icterus

Occasional (5-29%)HP:0032106

Intermittent yellowing of skin

Occasional (5-29%)HP:0001046

Abnormal skin colour

HP:0001000

Skeletal anomalies

HP:0000924

Related Conditions

Conjugated hyperbilirubinemia(parent)

Inherited disorder of bilirubin metabolism(parent)

Digestive system hereditary disorder(parent)

Hepatopathy(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Quick Facts

SNOMED CT: 32891000
UMLS CUI: C0220991
Fully Specified Name: Rotor syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.