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Lucey-driscoll Syndrome (disorder): Disease Bioinformatics

Research of Lucey-driscoll Syndrome (disorder) has been linked to Hyperbilirubinemia, Hereditary, Hyperbilirubinemia, Neonatal, Neonatal Jaundice, Kernicterus, Hyperbilirubinemia. The study of Lucey-driscoll Syndrome (disorder) has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Lucey-driscoll Syndrome (disorder) including antibodies and ELISA kits.

Lucey-driscoll Syndrome (disorder) Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Lucey-driscoll Syndrome (disorder) below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Related Diseases

Lucey-driscoll Syndrome (disorder) has been studied in relation to diseases such as:

Alternate Names

Lucey-driscoll Syndrome (disorder) is also known as Lucey-driscoll Syndrome, Transient Familial Neonatal Hyperbilirubinemia.