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GENE - TERM ANNOTATION REPORT

RGD ID: 3359
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Pmp22
Name: peripheral myelin protein 22
Acc ID: DOID:630
Term: genetic disease
Definition: A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/ "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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