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)
MIM:618505 - STOLERMAN NEURODEVELOPMENTAL SYNDROME; NEDSST

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0032790 - neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities