has characteristic has characteristic disease arises from structure disease arises from alteration in structure chromosome 5 (Human) mosaic trisomy 5 https://www.malacards.org/card/mosaic_trisomy_5 MEDGEN:419849 Mosaic trisomy type 5 GARD:0019301 Mosaic trisomy chromosome 5 MESH:C537762 Mosaic trisomy 5 is a rare chromosomal anomaly syndrome with a variable phenotype ranging from clinically normal to patients presenting intrauterine growth retardation, congenital heart anomalies (mainly ventricular septal defect), multiple dysmorphic features (e.g. hypertelorism, prominent nasal bridge) and other congenital anomalies (incl. eventration of diaphragm, agenesis of corpus callosum, cloverleaf skull, clinodactyly, anteriorly placed anus). Psychomotor development may be normal in spite of low growth parameters being associated. Orphanet:96060 trisomy 5 mosaicism SCTID:764629008 UMLS:C2931603 MONDO:0019866 chromosome 5 disorder mosaic trisomy