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neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language (DOID:0070050)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 20; mental retardation, autosomal dominant 20; MRD20
Alt IDs: OMIM:613443
Definition: An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay with hypotonia, poor motor development with limited walking, impaired intellectual development with poor or absent speech, and behavioral abnormalities and that has_material_basis_in an autosomal dominant mutation of the MEF2C gene on chromosome 5q14.3.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/17/2024
MGI 6.24 		The Jackson Laboratory