Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0060395 - chromosome 15q24 deletion syndrome


Disease Ontology 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.

Synonyms: 15q24 microdeletion syndrome

Xenbase Genes : sin3a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013256 - chromosome 15q24 deletion syndrome

OMIM:
OMIM:613406 - WITTEVEEN-KOLK SYNDROME; WITKOS

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), chromosomal deletion syndrome (is_a)