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GENE - TERM ANNOTATION REPORT

RGD ID: 619855
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Ddr2
Name: discoidin domain receptor tyrosine kinase 2
Acc ID: DOID:9002328
Term: FERGUSON-BONNI NEURODEVELOPMENTAL SYNDROME
Definition: This disease is an autosomal recessive disorder characterized by global developmental delay, impaired intellectual development, and hypotonia with early motor delay.
Definition Source(s): OMIM:619699
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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