Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | MYO15A | Pig | Alport syndrome | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Alport syndrome | ClinVar | PMID:28492532 and PMID:30311386 | MYO15A | Pig | autistic disorder | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autism | ClinVar | PMID:21681106 and PMID:30208311 | MYO15A | Pig | autosomal recessive nonsyndromic deafness | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16199547 more ... | MYO15A | Pig | autosomal recessive nonsyndromic deafness 3 | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10552926 more ... | MYO15A | Pig | Birt-Hogg-Dube syndrome | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Birt-Hogg-Dube syndrome | ClinVar | PMID:20188345 and PMID:28492532 | MYO15A | Pig | cleft palate | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cleft palate | ClinVar | PMID:24033266 more ... | MYO15A | Pig | common variable immunodeficiency 2 | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Immunodeficiency more ... | ClinVar | PMID:28492532 | MYO15A | Pig | congenital diaphragmatic hernia | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Agenesis of hemidiaphragm | ClinVar | PMID:24033266 more ... | MYO15A | Pig | Deafness, with Smith-Magenis Syndrome | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Deafness and with smith-magenis syndrome | ClinVar | PMID:11735029 more ... | MYO15A | Pig | Developmental Disabilities | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Global developmental delay | ClinVar | PMID:24033266 more ... | MYO15A | Pig | epilepsy | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Seizure | ClinVar | PMID:24033266 more ... | MYO15A | Pig | genetic disease | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:15654330 more ... | MYO15A | Pig | Hearing Loss | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16199547 more ... | MYO15A | Pig | Joubert syndrome 1 | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Familial aplasia of the vermis | ClinVar | PMID:28492532 | MYO15A | Pig | nonsyndromic deafness | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11735029 more ... | MYO15A | Pig | Potocki-Lupski syndrome | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Potocki-Lupski syndrome | ClinVar | PMID:28837307 | MYO15A | Pig | sensorineural hearing loss | | ISO | MYO15A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital sensorineural hearing impairment | ClinVar | PMID:17546645 more ... | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - OMIM
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