disease arises from structure disease arises from alteration in structure 8p (Human) syndrome caused by partial chromosomal deletion partial deletion of chromosome 8 partial deletion of the short arm of chromosome 8 https://github.com/monarch-initiative/mondo/issues/3664 https://www.malacards.org/card/partial_deletion_of_the_short_arm_of_chromosome_8 8p monosomy 8p deletion UMLS:C2931635 chromosome 8p deletion deletion 8p monosomy 8p partial monosomy of the short arm of chromosome 8 icd11.foundation:635585868 MESH:C537826 Chromosome 8p deletion is a chromosome abnormality that affects many different parts of the body. People with this condition are missing genetic material located on the short arm (p) of chromosome 8 in each cell. The severity of the condition and the associated signs and symptoms vary based on the size and location of the deletion and which genes are involved. Most cases are not inherited, although affected people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person. partial monosomy of chromosome 8p partial monosomy 8p partial deletion of chromosome 8p MONDO:0016890 Orphanet:261920 partial deletion of the short arm of chromosome type 8 MEDGEN:444105