Term Name: | autosomal dominant intellectual developmental disorder 21 |
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Synonyms: | autosomal dominant mental retardation 21, autosomal dominant non-syndromic intellectual disability 21, MRD21 |
Definition: | An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CTCF gene on chromosome 16q22.1. |
Ontology: | Human Disease [DOID:0070051] ( DOID:0070051 ) |