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GENE - TERM ANNOTATION REPORT

RGD ID: 1595998
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Tnfrsf13b
Name: TNF receptor superfamily member 13B
Acc ID: DOID:0080006
Term: bone development disease
Definition: A bone disease that results_in abnormal growth and development located_in bone or located_in cartilage. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Dysplasia "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.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
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