Human genes for chromosome 15q13.3 microdeletion syndrome
Chromosome 15q13.3 microdeletion syndrome [DOID:0060394]
A chromosomal deletion syndrome that is characterized by intellectual dsability, developmental delay, autism spectrum disorder and seizure, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15.
Synonyms: chromosome 15q13.3 microdeletion syndrome, chromosome 15q133 microdeletion syndrome, chromosome 15q13.3 microdeletion disease, chromosome 15q13.3 microdeletion disorder, DOID:0060394 ...