has characteristic has characteristic disease arises from structure disease arises from alteration in structure chromosome 9 (Human) mosaic trisomy 9 https://rarediseases.info.nih.gov/diseases/43/mosaic-trisomy-9 https://www.malacards.org/card/mosaic_trisomy_9 MONDO:0020490 Orphanet:99776 GARD:0000043 trisomy 9 mosaicism NORD:966 Mosaic trisomy 9 is a chromosomal abnormality that can affect may parts of the body. In people affected by this condition, some of the body's cells have three copies of chromosome 9 (trisomy), while other cells have the usual two copies of this chromosome. The signs and symptoms vary but may include mild to severe intellectual disability, developmental delay, growth problems (both before and after birth), congenital heart defects, and/or abnormalities of the craniofacial (skull and face) region. Most cases are not inherited; it often occurs sporadically as a random event during the formation of the reproductive cells (egg and sperm) or as the fertilized egg divides. Treatment is based on the signs and symptoms present in each person. Mosaic trisomy type 9 Mosaic trisomy chromosome 9 MEDGEN:419661 SCTID:764989007 UMLS:C2930908 MESH:C535454 chromosome 9 disorder mosaic trisomy