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Gorlin-chaudhry-moss Syndrome: Disease Bioinformatics

Research of Gorlin-chaudhry-moss Syndrome has been linked to Hypertrichosis, Craniosynostosis, Craniofacial Dysostosis, Patent Ductus Arteriosus, Craniofacial Abnormalities. The study of Gorlin-chaudhry-moss Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Gorlin-chaudhry-moss Syndrome has been researched in relation to the Ossification Pathway. This pathway complements our catalog of research reagents for the study of Hypertrichosis, Craniosynostosis, Craniofacial Dysostosis, Patent Ductus Arteriosus, Craniofacial Abnormalities.

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

Related Pathways

Gorlin-chaudhry-moss Syndrome has been linked to:

Alternate Names

Gorlin-chaudhry-moss Syndrome is also known as gorlin chaudhry moss syndrome, craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies, gorlin-chaudhry-moss syndrome, gcm syndrome.