has characteristic has characteristic disease arises from structure disease arises from alteration in structure chromosome 10 (Human) mosaic trisomy 10 https://www.malacards.org/card/mosaic_trisomy_10 Mosaic trisomy 10 is a rare chromosomal anomaly syndrome, with a highly variable phenotype, principally characterized by growth delay, craniofacial dysmorphism (incl. prominent forehead, hypertelorism, upslanting palpebral fissures, blepharophimosis, low-set malformed large ears, high arched palate, cleft lip/palate, retrognathia) and cardiac, renal and skeletal (e.g. radial ray defects, scoliosis) malformations, with death usually occurring neonatally or in early infancy. Other reported features include central nervous system and ear anomalies, as well as facial clefts and anal atresia. mosaic trisomy 10 GARD:0019302 uniparental disomy of 10 Mosaic trisomy chromosome 10 Orphanet:96063 SCTID:764461004 MESH:C538292 trisomy 10 mosaicism Mosaic trisomy type 10 chromosome 10, uniparental disomy UMLS:C2931794 MONDO:0019868 MEDGEN:419163 chromosome 10 disorder mosaic trisomy