About   Help   FAQ
Disease Ontology Browser
autosomal dominant intellectual developmental disorder 7 (DOID:0070037)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 7; autosomal dominant non-syndromic intellectual disability 7; DYRK1A syndrome; MRD7
Alt IDs: OMIM:614104
Definition: An autosomal dominant intellectual developmental disorder that is characterized by intellectual disability including impaired speech development, autism spectrum disorder including anxious and/or stereotypic behavior problems, and microcephaly and that has_material_basis_in an autosomal dominant mutation of the DYRK1A gene on chromosome 21q22.13.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory