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 (1)
OMIM:615834 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26


Xenbase Genes: auts2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014361 - autism spectrum disorder due to AUTS2 deficiency

Disease Ontology (DO):
DOID:0070056 - autosomal dominant non-syndromic intellectual disability 26