The annotation has been inferred from sequence orthology with SCN10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
125 RGD objects have been annotated to Brugada syndrome (DOID:0050451)
12 papers in RGD have been used to annotate Scn10a
Curation Notes: ClinVar Annotator: match by term: Brugada syndrome | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome
The annotation has been inferred from sequence orthology with SCN10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
125 RGD objects have been annotated to Brugada syndrome (DOID:0050451)
12 papers in RGD have been used to annotate Scn10a
Curation Notes: ClinVar Annotator: match by term: Brugada syndrome | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS)
The annotation has been inferred from sequence orthology with SCN10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
125 RGD objects have been annotated to Brugada syndrome (DOID:0050451)
12 papers in RGD have been used to annotate Scn10a
Curation Notes: ClinVar Annotator: match by term: Brugada syndrome | ClinVar Annotator: match by term: Brugada syndrome, lidocaine-induced | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome
The annotation has been inferred from sequence orthology with SCN10A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
125 RGD objects have been annotated to Brugada syndrome (DOID:0050451)
12 papers in RGD have been used to annotate Scn10a
Curation Notes: ClinVar Annotator: match by term: Brugada syndrome | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome