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:615866 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND WITH OR WITHOUT OCULAR MALFORMATIONS OR HYPOGONADOTROPIC HYPOGONADISM; IDDMOH

Xenbase Genes: sox11

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014376 - intellectual disability, autosomal dominant 27
MONDO:0015452 - Coffin-Siris syndrome

Disease Ontology (DO):
DOID:0070057 - Coffin-Siris syndrome 9