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GENE - TERM ANNOTATION REPORT

RGD ID: 1323630
Species: Homo sapiens
RGD Object: Gene
Symbol: CHD7
Name: chromodomain helicase DNA binding protein 7
Acc ID: DOID:9003232
Term: Kallmann Syndrome 5
Definition: null
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)
CHD7 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Kallmann syndrome 5PMID:22461308 PMID:25741868 PMID:28492532 PMID:30311386
CHD7 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Kallmann syndrome 5PMID:25741868 PMID:28492532
CHD7 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Kallmann syndrome 5PMID:17576681 PMID:18834967 PMID:25741868 PMID:28492532 PMID:29419413 PMID:30311386 PMID:34837038 PMID:9536098
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