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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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory