Human genes for chromosome 15q11.2 deletion syndrome
Chromosome 15q11.2 deletion syndrome [DOID:0060393]
A chromosomal deletion syndrome that is characterized by intellectual disbaility, dysmorphic facies, psychiatric illness and autism spectrum disorder, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15.
Synonyms: chromosome 15q11.2 deletion syndrome, chromosome 15q112 deletion syndrome, chromosome 15q11.2 deletion disease, chromosome 15q11.2 deletion disorder, DOID:0060393 ...