disease arises from structure disease arises from alteration in structure 6pter-p24 (Human) syndromic intellectual disability syndrome caused by partial chromosomal deletion iridogoniodysgenesis chromosome 6pter-p24 deletion syndrome https://github.com/monarch-initiative/mondo/issues/3664 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5588 https://www.malacards.org/card/chromosome_6pter_p24_deletion_syndrome chromosome 6pter-p24 deletion syndrome, isolated cases Orphanet:96125 distal monosomy type 6p 6p25 microdeletion syndrome 6p subtelomeric deletion syndrome OMIM:612582 distal deletion 6p MEDGEN:393396 SCTID:718688008 MESH:C567239 Distal monosomy 6p is responsible for a distinct chromosome deletion syndrome with a recognizable clinical picture including intellectual deficit, ocular abnormalities, hearing loss, and facial dysmorphism. MONDO:0012948 DOID:0060422 monosomy 6p25 chromosome 6pter-p24 deletion syndrome GARD:0016845 UMLS:C2675486 multiple congenital anomalies/dysmorphic syndrome-intellectual disability partial deletion of the short arm of chromosome 6