Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | autosomal dominant nonsyndromic deafness 56 | | ISO | TNC (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:21681106 more ... | genetic disease | | ISO | TNC (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:30311386 | Hearing Loss | | ISO | TNC (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hearing impairment | ClinVar | PMID:30311386 | hereditary breast ovarian cancer syndrome | | ISO | TNC (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome | ClinVar | PMID:25741868 | myopia | | ISO | TNC (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Myopia | ClinVar | PMID:25741868 | sensorineural hearing loss | | ISO | TNC (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Progressive sensorineural hearing impairment | ClinVar | PMID:25741868 | Vertigo | | ISO | TNC (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Vertigo | ClinVar | PMID:25741868 | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - CTD
Imported Disease Annotations - OMIM
Gene Ontology Annotations Click to see Annotation Detail View
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