Bilirubin Metabolic Disorder

Alias:
Hyperbilirubinemia
Hereditary Hyperbilirubinemia
Hyperbilirubinemia, Hereditary
Hyperbilirubinaemia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Bilirubin Metabolic Disorder, also known as hyperbilirubinemia, is related to gilbert syndrome and crigler-najjar syndrome, type i, and has symptoms including icterus, polydipsia and muscle weakness. An important gene associated with Bilirubin Metabolic Disorder is UGT1A1 (UDP Glucuronosyltransferase Family 1 Member A1), and among its related pathways/superpathways are Metabolism and Metapathway biotransformation Phase I and II. The drugs Oxytocin and Ritonavir have been mentioned in the context of this disorder. Affiliated tissues include liver and bone marrow.
Related ID:
MESH:D006932

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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114
1003
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Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
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Publications
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References Literature

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