disease has basis in dysfunction of PUF60 8q24.3 microdeletion syndrome GARD:0012814 MONDO:0014263 OMIM:615583 Orphanet:508488 UMLS:C3810023 VRJS Verheij syndrome chromosome 8Q24.3 deletion syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability malformation syndrome with short stature rare syndrome with cardiac malformations partial deletion of the long arm of chromosome 8 syndromic renal or urinary tract malformation genetic multiple congenital anomalies/dysmorphic syndrome