autosomal dominant intellectual developmental disorder 11 (DOID:0070041)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 11; autosomal dominant non-syndromic intellectual disability 11; MRD11
Alt IDs: OMIM:614257
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the EPB41L1 gene on chromosome 20q11.23.