About   Help   FAQ
Disease Ontology Browser
autosomal dominant intellectual developmental disorder 29 (DOID:0070059)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 29; autosomal dominant non-syndromic intellectual disability 29; MRD29
Alt IDs: OMIM:616078
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the SETBP1 gene on chromosome 18q12.3.


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
04/16/2024
MGI 6.23
The Jackson Laboratory