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autosomal dominant intellectual developmental disorder 39 (DOID:0070069)
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Synonyms: autosomal dominant mental retardation 39; autosomal dominant non-syndromic intellectual disability 39; MRD39
Alt IDs: OMIM:616521
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant heterozygous mutation in the MYT1L gene on chromosome 2p25.3.

Disease References using Mouse Models (2)
Contributing Projects:
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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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory