has material basis in germline mutation in disease arises from structure disease arises from alteration in structure SIN3A 15q24 (Human) syndromic intellectual disability syndrome caused by partial chromosomal deletion hereditary disease chromosome 15q24 deletion syndrome https://github.com/monarch-initiative/mondo/issues/3664 https://github.com/monarch-initiative/mondo/issues/5588 https://www.malacards.org/card/chromosome_15q24_deletion_syndrome https://www.malacards.org/card/witteveen_kolk_syndrome monosomy 15q24 DECIPHER:66 GARD:0012219 OMIM:613406 chromosome 15q24 deletion syndrome DOID:0060395 Del(15)(q24) 15q24 recurrent microdeletion syndrome 15q24 microdeletion syndrome MONDO:0013256 MESH:C579849 WITKOS SCTID:699308002 15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies. UMLS:C3150674 Orphanet:94065 MEDGEN:462024 multiple congenital anomalies/dysmorphic syndrome-intellectual disability partial deletion of the long arm of chromosome 15