Summary

Perlman Syndrome, also known as nephroblastomatosis, fetal ascites, macrosomia and wilms tumor,is related to fetal macrosomia and myeloproliferative neoplasms, familial,and has symptoms including tall stature, open mouth and macrocephaly. An important gene associated with Perlman Syndrome is DIS3L2 (DIS3 Like 3'-5' Exoribonuclease 2), and among its related pathways are Diseases associated with O-glycosylation of proteins and Type II diabetes mellitus. Affiliated tissues include myeloid, kidney and bone

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Symptoms Associated With Trait