Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal urinary color
Very frequent (80-99%)HP:0012086
Biliary tract disease
Very frequent (80-99%)HP:0001080
Conjugated hyperbilirubinemia
Very frequent (80-99%)HP:0002908
Liver disease
Very frequent (80-99%)HP:0001392
Yellowing of the skin
Very frequent (80-99%)HP:0000952
Abnormal gastric mucosa morphology
Frequent (30-79%)HP:0004295
Abdominal discomfort
Occasional (5-29%)HP:0002027
Enlarged liver
Occasional (5-29%)HP:0002240
Haemorrhagic disorders
Occasional (5-29%)HP:0001928
Pyrexia
Occasional (5-29%)HP:0001945
Tiredness
Occasional (5-29%)HP:0012378
Related Conditions
Conjugated hyperbilirubinemia(parent)
Recessive hereditary disorder (autosomal)(parent)
Inherited disorder of bilirubin metabolism(parent)
Congenital anomaly of liver(parent)
Disorder of pigmentation(parent)
Digestive system hereditary disorder(parent)
Lesion of liver(parent)
Metabolic and genetic disorder affecting the liver(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 44553005
- UMLS CUI
- C0022350
- Fully Specified Name
- Dubin-Johnson syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 11
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.