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GENE - TERM ANNOTATION REPORT

RGD ID: 736625
Species: Homo sapiens
RGD Object: Gene
Symbol: PRPS1
Name: phosphoribosyl pyrophosphate synthetase 1
Acc ID: DOID:9004538
Term: Hearing Loss
Definition: A general term for the complete or partial loss of the ability to hear from one or both ears.
Definition Source(s): MESH:D034381
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)
PRPS1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: X-linked nonsyndromic hearing loss 
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