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GENE - TERM ANNOTATION REPORT

RGD ID: 621546
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Tpm3
Name: tropomyosin 3
Acc ID: DOID:0080102
Term: congenital myopathy 4A
Definition: A congenital myopathy that is characterized by skeletal muscle weakness, particularly in the muscles of the shoulders, upper arms, hips, and thighs. (DO)
Definition Source(s): https://ghr.nlm.nih.gov/condition/congenital-fiber-type-disproportion "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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