Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Brugada syndrome | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11527630 more ... | Brugada syndrome | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11527630 more ... | Brugada syndrome | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11527630 more ... | Brugada syndrome | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11527630 more ... | Brugada syndrome 1 | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Right bundle branch block more ... | ClinVar | PMID:24998131 more ... | erythromelalgia | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sodium channelopathy-related small fiber neuropathy | ClinVar | PMID:25741868 and PMID:28492532 | familial episodic pain syndrome 2 | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Episodic pain syndrome more ... | ClinVar | PMID:17576681 more ... | genetic disease | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:11527630 more ... | hereditary sensory and autonomic neuropathy type 7 | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary sensory and autonomic neuropathy type 7 | ClinVar | PMID:28492532 | Marsili syndrome | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Impaired thermal sensitivity | ClinVar | PMID:25741868 more ... | Sudden Unexpected Nocturnal Death Syndrome | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden unexpected nocturnal death syndrome | ClinVar | PMID:11527630 more ... | Visceral Heterotaxy 4, Autosomal | | ISO | SCN10A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Heterotaxy more ... | ClinVar | PMID:28492532 | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - CTD
Imported Disease Annotations - OMIM
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