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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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory