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Disease Ontology Browser
GAND syndrome (DOID:0070048)
Alliance: disease page
Synonyms: autosomal dominant intellectual developmental disorder 18; autosomal dominant mental retardation 18; autosomal dominant non-syndromic intellectual disability 18; MRD18
Alt IDs: OMIM:615074
Definition: An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay apparent from infancy, with motor delay and moderate to severely impaired intellectual development and that has_material_basis_in an autosomal dominant mutation of the GATAD2B gene on chromosome 1q21.3.

Disease References using Mouse Models (1)
Contributing Projects:
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