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autosomal dominant non-syndromic intellectual disability 29 (DOID:0070059)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 29; MRD29
Alt IDs: OMIM:616078
Definition: An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of SETBP1 on chromosome 18q12.3.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/16/2018
MGI 6.12
The Jackson Laboratory