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chromosome 15q24 deletion syndrome (DOID:0060395)
Alliance: disease page
Synonyms: 15q24 microdeletion syndrome
Alt IDs: OMIM:613406, ICD10CM:Q93.5, MESH:C579849, ORDO:94065
Definition: A chromosomal deletion syndrome that is characterized by dysmorphic facial features, intellectual disability and seizure, has_material_basis_in autosomal dominant inheritance of mutation in the SIN3A gene causing partial deletion of the long arm of chromosome 15.

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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
MGI 6.13
The Jackson Laboratory