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.