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:613443 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL

Xenbase Genes: mef2c

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013266 - intellectual disability, autosomal dominant 20
MONDO:0016456 - 5q14.3 microdeletion syndrome

Disease Ontology (DO):
DOID:0070050 - neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language