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


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/05/2019
MGI 6.13
The Jackson Laboratory