About   Help   FAQ
Disease Ontology Browser
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.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory