autosomal dominant intellectual developmental disorder 19 (DOID:0070049)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 19; autosomal dominant non-syndromic intellectual disability 19; MRD19
Alt IDs: OMIM:615075
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CTNNB1 gene on chromosome 3p22.1.