disease has basis in dysfunction of DIS3L2 syndromic disease Perlman syndrome DOID:0060476 GARD:0003936 ICD10:Q87.3 MESH:C536399 MONDO:0009965 NCIT:C103144 OMIM:267000 Orphanet:2849 PRLMNS Perlman syndrome Perlman syndrome is characterized principally by polyhydramnios, neonatal macrosomia, bilateral renal tumours (hamartomas with or without nephroblastomatosis), hypertrophy of the islets of Langerhans and facial dysmorphism. SCTID:722231005 UMLS:C0796113 https://rarediseases.info.nih.gov/diseases/3936/perlman-syndrome nephroblastomatosis - fetal ascites - macrosomia - Wilms tumor nephroblastomatosis fetal ascites macrosomia and Wilms tumor nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor nephroblastomatosis, fetal ascites, macrosomia, and Wilms tumor nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome renal hamartomas, nephroblastomatosis and fetal gigantism renal hamartomas, nephroblastomatosis, and fetal gigantism polymalformative genetic syndrome with increased risk of developing cancer inherited renal cancer-predisposing syndrome overgrowth syndrome