01
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Gilbert Disease (Disorder)
- Standard Disease Name
- gilbert disease (disorder)
- MeSH Tree
- No data
- ICD-10
- E80.4
Identifiers
- DO ID
- No data
- MeSH ID
- D005878
- OMIM ID
- 191740|143500|MTHU031877
- UMLS ID
- C0017551
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.|MSH2017_2016_08_12:A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Ingredients
target disease -> ingredient target8 Ingredients