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autosomal dominant intellectual developmental disorder 3 (DOID:0070033)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 3; autosomal dominant non-syndromic intellectual disability 3; MRD3
Alt IDs: OMIM:612580
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CDH15 gene on chromosome 16q24.3.


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)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory