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Summary Literature (0)
OMIM:613443 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL


Xenbase Genes: mef2c

Human Disease Resource: OMIM

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

Disease Ontology (DO):
DOID:0070050 - mental retardation, autosomal dominant 20