disease arises from structure disease arises from alteration in structure 6p (Human) syndrome caused by partial chromosomal duplication partial duplication of chromosome 6 partial duplication of the short arm of chromosome 6 https://github.com/monarch-initiative/mondo/issues/3492 https://www.malacards.org/card/partial_duplication_of_the_short_arm_of_chromosome_6 Orphanet:262740 trisomy 6p partial duplication of chromosome 6p MESH:C537811 partial duplication of the short arm of chromosome type 6 icd11.foundation:657610285 Duplication 6p Chromosome 6p duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the short arm (p) of chromosome 6. The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved. Features that often occur in people with chromosome 6p duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features. This condition can occur sporadically or be inherited from a parent who is either mildy affected (has the deletion) or carries a balanced translocation. Treatment is based on the signs and symptoms present in each person. UMLS:C5679721 partial trisomy of chromosome 6p 6p duplication chromosome 6p duplication MONDO:0016943 MEDGEN:1826043 6p trisomy partial trisomy of the short arm of chromosome 6 partial trisomy 6p