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GENE - TERM ANNOTATION REPORT

RGD ID: 12584988
Species: Ictidomys tridecemlineatus
RGD Object: Gene
Symbol: Dis3l2
Name: DIS3 like 3'-5' exoribonuclease 2
Acc ID: DOID:0060476
Term: Perlman syndrome
Definition: A syndrome characterized by polyhydramnios with neonatal macrosomia, nephromegaly, distinctive facial appearance, renal dysplasia, nephroblastomatosis, and predisposition to Wilms tumor. It shows similarities to Beckwith-Wiedemann syndrome. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/Perlman_syndrome "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/18780370 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/22306653 "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
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