has characteristic has characteristic disease arises from structure disease arises from alteration in structure chromosome 15 (Human) mosaic trisomy 15 https://www.malacards.org/card/mosaic_trisomy_15 Mosaic trisomy 15 is a rare chromosomal anomaly syndrome principally characterized by intrauterine growth restriction, congenital cardiac anomalies (incl. ventricular and atrial septal defects, patent ductus arteriosus) and craniofacial dysmorphism (incl. hypertelorism, downslanting palpebral fissures, wide nasal bridge). Patients also present brain (e.g. hypoplastic cerebellum, ventricular asymmetry), renal (e.g. small dysplastic kidneys), and/or genital (undescended testis, small penis, hypoplastic labia majora) anomalies. Digital and skin pigmentation abnormalities have also been reported. SCTID:764619001 chromosome 15, trisomy mosaicism MONDO:0015727 UMLS:C2931707 GARD:0005313 Mosaic trisomy chromosome 15 MESH:C538037 trisomy 15 mosaicism MEDGEN:419475 Mosaic trisomy type 15 Orphanet:1706 chromosome 15 disorder mosaic trisomy