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GENE - TERM ANNOTATION REPORT

RGD ID: 1349710
Species: Homo sapiens
RGD Object: Gene
Symbol: GPR34
Name: G protein-coupled receptor 34
Acc ID: DOID:9001153
Term: FG Syndrome 4
Definition: This disease is an X-linked recessive intellectual developmental disorder characterized by congenital hypotonia, constipation, behavioral disturbances, and dysmorphic features.
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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