Submit your image related to Diseases to be featured!
Submit your Twitter account related to Tukel Syndrome to be featured!
Submit your blog on Tukel Syndrome to be featured!
||Submit your event on Tukel Syndrome to be featured!
Submit your video on Tukel Syndrome to be featured!
Submit your charity on Tukel Syndrome to be featured!
Tukel Syndrome: Disease Bioinformatics
Research of Tukel Syndrome has been linked to Ophthalmoplegia, Fibrosis, Blepharoptosis, Ocular Motility Disorders, Congenital Hand Deformities. The study of Tukel Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Tukel Syndrome has been researched in relation to the Limb Development Pathway. This pathway complements our catalog of research reagents for the study of Ophthalmoplegia, Fibrosis, Blepharoptosis, Ocular Motility Disorders, Congenital Hand Deformities.
Tukel 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 Tukel Syndrome below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
Tukel Syndrome has been linked to:
Tukel Syndrome has been studied in relation to diseases such as:
Alternate NamesTukel Syndrome is also known as Congenital Extraocular Muscle Fibrosis With Ulnar Hand Anomalies.