Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Autosomal Dominant Nonsyndromic Deafness 90 | | ISO | MYO3A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Deafness and autosomal dominant 90 | ClinVar | PMID:25741868 more ... | autosomal recessive nonsyndromic deafness 30 | | ISO | MYO3A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:12032315 more ... | genetic disease | | ISO | MYO3A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:24033266 more ... | Hearing Loss | | ISO | MYO3A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:24033266 more ... | nonsyndromic deafness | | ISO | MYO3A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Nonsyndromic hearing loss and deafness | ClinVar | PMID:25741868 more ... | Nonsyndromic Sensorineural Hearing Loss | | ISO | MYO3A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: nonsyndromic sensorineural hearing loss | ClinVar | PMID:25741868 more ... | sensorineural hearing loss | | ISO | MYO3A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sensorineural hearing loss disorder | ClinVar | PMID:12032315 more ... | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - OMIM
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