About   Help   FAQ
Disease Ontology Browser
autosomal dominant intellectual developmental disorder 11 (DOID:0070041)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 11; autosomal dominant non-syndromic intellectual disability 11; MRD11
Alt IDs: OMIM:614257
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the EPB41L1 gene on chromosome 20q11.23.

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