How to use?
1. Gene query -
basic information about the gene
2. Query syndrome -
CS* information of the syndrome and a link to find it's related
3. Find related genes -
finding related genes using a query set of genes with the
ability of choosing (filtering) an area of the genome (using genes, SNP's or
chromosome and physical location) as the place to look for related genes (good for
4. Cross syndromes -
finding related syndromes using a set of chosen syndromes.
5. Query tree -
going over the MeSH entries tree to look for syndromes having CS
related to them.
6. Build syndrome -
build an artificial syndrome which is a group of selected CS
phrases found in the database and find its related syndromes (good for unknown or
new syndromes and also for reducing the phenotypes from a known syndrome).
* CS - Clinical Synopsis (OMIM phenotypes)