chromosome 15q24 deletion syndrome

Summary

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: sin3a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013256 - chromosome 15q24 deletion syndrome

MONDO:0013256 - chromosome 15q24 deletion syndrome

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)