disease arises from structure disease arises from alteration in structure 7p (Human) syndrome caused by partial chromosomal deletion partial deletion of chromosome 7 partial deletion of the short arm of chromosome 7 https://github.com/monarch-initiative/mondo/issues/3664 https://www.malacards.org/card/partial_deletion_of_the_short_arm_of_chromosome_7 7p deletion 7p monosomy partial monosomy 7p partial deletion of the short arm of chromosome type 7 icd11.foundation:1523142467 UMLS:C5679668 monosomy 7p MEDGEN:1826021 Chromosome 7p deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the short arm (p) of chromosome 7. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with chromosome 7p deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. Most cases are not inherited, but people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person. partial deletion of chromosome 7p deletion 7p chromosome 7p deletion partial monosomy of chromosome 7p Orphanet:261911 MONDO:0016889 partial monosomy of the short arm of chromosome 7