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GENE - TERM ANNOTATION REPORT

RGD ID: 62030
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Myh7
Name: myosin heavy chain 7
Acc ID: DOID:3827
Term: congenital diaphragmatic hernia
Definition: A diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Congenital_diaphragmatic_hernia "DO" "DO", http://ghr.nlm.nih.gov/condition/congenital-diaphragmatic-hernia "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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