Term Name:	autosomal dominant intellectual developmental disorder 39
Synonyms:	autosomal dominant mental retardation 39, autosomal dominant non-syndromic intellectual disability 39, MRD39
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.
Ontology:	Human Disease [DOID:0070069]   ( DOID:0070069 )