Term Name:	autosomal dominant intellectual developmental disorder 19
Synonyms:	autosomal dominant mental retardation 19, autosomal dominant non-syndromic intellectual disability 19, MRD19
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CTNNB1 gene on chromosome 3p22.1.
Ontology:	Human Disease [DOID:0070049]   ( DOID:0070049 )