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Gombo Syndrome: Disease Bioinformatics

Gombo syndrome is a rare syndrome characterized by a Small head, small eyes, abnormally short fingers, severe mental retardation, and delayed physical growth at puberty. This is listed as a rare diseases it effects roughly one out of every 200,000 people.

Gombo Syndrome 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 Gombo Syndrome below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

Related Genes

Related Pathways

Related PTMs

Alternate Names

Gombo Syndrome is also known as Growth Retardation, Ocular Abnormalities, Microcephaly, Brachydactyly, And Oligophrenia.