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:601358 - NICOLAIDES-BARAITSER SYNDROME; NCBRS

Xenbase Genes: smarca2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011053 - intellectual disability-sparse hair-brachydactyly syndrome