autosomal dominant intellectual developmental disorder 21 (DOID:0070051)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 21; autosomal dominant non-syndromic intellectual disability 21; MRD21
Alt IDs: OMIM:615502
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CTCF gene on chromosome 16q22.1.