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Hyperbilirubinemia
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
UGT1A1
ABCC2
LST1
SLCO1B1
SLCO1B3
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
antibiotic metabolic process
flavonoid glucuronidation
MIKKELSEN_IPS_LCP_WITH_H3K27ME3
TAKAYAMA_BOUND_BY_AR
xenobiotic glucuronidation
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Curated Studies
Most Correlated Studies
Genome wide expression in ADAMTS13-deficient thrombotic thrombocytopenic purpura TTP
CD4+ T cells from an atypical hemolytic uremic syndrome (aHUS) patient carrying mutant CD46
Mouse Phenotypes - Thrombocytopenia
Mouse Phenotypes - Autosomal recessive hereditary disorder
OMIM - Porphyria
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Literature
Most Relevant Literature
Neonatal Hyperbilirubinemia.
Intravenous immunoglobulin G therapy for neonatal hyperbilirubinemia.
Diagnostic and predictive ability of hyperbilirubinemia severity in cats: A multicenter retrospectiv…
Neonatal hyperbilirubinemia and repercussions on neurodevelopment: A systematic review.
Severe neonatal hyperbilirubinaemia: lessons learnt from a national perinatal audit.
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Clinical Trials
Most Relevant Clinical Trials
Prediction of Neonatal Hyperbilirubinemia
The Predictors of the Neonatal Hyperbilirubinemia
Multi-center Clinical Study on Neonatal Hyperbilirubinemia
Transcutaneous Screening for Risk of Severe Hyperbilirubinemia in South African Newborns
Is Primiparity a Risk Factor for Neonatal Hyperbilirubinemia?
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