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autosomal dominant intellectual developmental disorder 46 (DOID:0080237)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 46
Alt IDs: OMIM:617601
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the KCNQ5 gene on chromosome 6q14.


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
11/12/2024
MGI 6.24
The Jackson Laboratory