Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:613444 - CHROMOSOME 16p11.2 DELETION SYNDROME, 220-KB

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013267 - distal 16p11.2 microdeletion syndrome

Disease Ontology (DO):
DOID:0060398 - chromosome 16p11.2 deletion syndrome, 220-kb