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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

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

In Mondo Disease Ontology:
MONDO:0013256 - chromosome 15q24 deletion syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : sin3a

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), chromosomal deletion syndrome (is_a)