Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | autosomal dominant nonsyndromic deafness | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autosomal dominant non-syndromic sensorineural deafness type DFNA | ClinVar | PMID:25741868 | autosomal dominant nonsyndromic deafness 22 | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11167014 more ... | autosomal recessive nonsyndromic deafness 37 | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11167014 more ... | essential tremor | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Essential tremor | ClinVar | PMID:12687499 more ... | genetic disease | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:11167014 more ... | Hearing Loss | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:17576681 more ... | Hearing Loss | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:12687499 more ... | male infertility | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Male infertility | ClinVar | PMID:17576681 more ... | nonsyndromic deafness | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:12687499 more ... | Nonsyndromic Sensorineural Hearing Loss | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss and Dominant | ClinVar | PMID:25741868 and PMID:28492532 | Sensorineural Deafness with Hypertrophic Cardiomyopathy | | ISO | MYO6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sensorineural deafness with hypertrophic cardiomyopathy | ClinVar | PMID:15060111 more ... | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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