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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:3614
Term: Kallmann syndrome
Definition: A hypogonadotropic hypogonadism with a defective sense of smell (anosmia or hyposmia). (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/26194704 "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.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
CHD7 EXP 11554173CTDCTD Direct Evidence: marker/mechanism 
CHD7 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hypogonadism with anosmia 
CHD7 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hypogonadism with anosmiaPMID:25741868 PMID:28492532
CHD7 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hypogonadism with anosmiaPMID:28492532
CHD7 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hypogonadism with anosmiaPMID:18414213 PMID:18445044 PMID:21158681 PMID:22461308 PMID:24033266 PMID:25077900 PMID:25741868 PMID:26467025 PMID:28475860 PMID:28492532 PMID:29304373
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