DO_rare_slim has material basis in autosomal dominant disease chromosomal deletion syndrome chromosome 17q12 deletion syndrome disease_ontology A chromosomal deletion syndrome that has_material_basis_in a chromosome 17q12 deletion and that is characterized by renal cystic disease, maturity onset diabetes of the young type 5, cognitive impairment, developmental delay (particularly of speech), autistic traits and autism spectrum disorder. ICD10CM:Q93.5 ORDO:261265 2015-09-28T16:55:38Z MIM:614527 GARD:13297 DOID:0060404 17q12 microdeletion syndrome autosomal dominant inheritance