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GENE - TERM ANNOTATION REPORT

RGD ID: 1318463
Species: Homo sapiens
RGD Object: Gene
Symbol: SDHB
Name: succinate dehydrogenase complex iron sulfur subunit B
Acc ID: DOID:6457
Term: Cowden syndrome
Definition: A PTEN hamartoma tumor syndrome that is characterized by multiple noncancerous, tumor-like growths (hamartomas) and an increased risk of certain forms of cancer, especially breast, thyroid and endometrium. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Cowden_syndrome "DO" "DO", http://ghr.nlm.nih.gov/condition/cowden-syndrome "DO" "DO", http://rarediseases.info.nih.gov/gard/6202/cowden-syndrome/resources/1 "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)
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden syndromePMID:25741868 PMID:28492532 PMID:34906457
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden syndromePMID:23660872 PMID:25741868 PMID:26269449 PMID:28492532
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden syndromePMID:25741868 PMID:28229225 PMID:28492532 PMID:34309460 PMID:34906457
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden's syndromePMID:11404820 PMID:16314641 PMID:16317055 PMID:17987308 PMID:19454582 PMID:19802898 PMID:22517554 PMID:22995128 PMID:23072324 PMID:25741868 PMID:28492532 PMID:30155846 PMID:30877234
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden syndromePMID:25741868 PMID:26729832 PMID:28492532
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden syndromePMID:25741868 PMID:28492532
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden's syndromePMID:25741868 PMID:27604842 PMID:28492532 PMID:34490615
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden syndrome 
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden's syndromePMID:18678321 PMID:19368708 PMID:22703879 PMID:24033266 PMID:24728327 PMID:25741868 PMID:28492532
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden's syndromePMID:14985401 PMID:16322339 PMID:16912137 PMID:17102082 PMID:17102083 PMID:17298551 PMID:17639058 PMID:18551016 PMID:18678321 PMID:19368708 PMID:19399650 PMID:19802898 PMID:21979946 PMID:22703879 PMID:22995991 PMID:23666964 PMID:24728327 PMID:25333069 PMID:25694510 PMID:25741868 PMID:26092435 PMID:28492532
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden syndromePMID:22703879 PMID:25741868 PMID:28492532
SDHB IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cowden syndromePMID:17376234 PMID:21979946 PMID:24033266 PMID:24728327 PMID:25741868 PMID:28492532
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