has material basis in germline mutation in disease arises from structure disease arises from alteration in structure PUF60 8q24.3 (Human) syndrome caused by partial chromosomal deletion 8q24.3 microdeletion syndrome https://github.com/monarch-initiative/mondo/issues/3664 https://www.malacards.org/card/verheij_syndrome GARD:0012814 Orphanet:508488 OMIM:615583 chromosome 8Q24.3 deletion syndrome MEDGEN:816353 VRJS UMLS:C3810023 Verheij syndrome MONDO:0014263 multiple congenital anomalies/dysmorphic syndrome-intellectual disability partial deletion of the long arm of chromosome 8 cardiogenetic disease