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-Chemical Interaction Annotations Click to see Annotation Detail View
Gene Ontology Annotations Click to see Annotation Detail View
Biological Process
Cellular Component
Molecular Function
Molecular Pathway Annotations Click to see Annotation Detail View
