Human genes for chromosome 15q24 deletion syndrome
Chromosome 15q24 deletion syndrome [DOID:0060395]
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: chromosome 15q24 deletion syndrome, chromosome 15q24 deletion disease, chromosome 15q24 deletion disorder, DOID:0060395, 15q24 microdeletion syndrome ...