Term Name: | autosomal dominant intellectual developmental disorder 19 |
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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 ) |