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Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | ATF6 | Human | achromatopsia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia | ClinVar | PMID:16199547 more ... | ATF6 | Human | achromatopsia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia | ClinVar | PMID:24033266 | ATF6 | Human | achromatopsia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia | ClinVar | PMID:28041643 | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 and PMID:28492532 | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 and PMID:30202406 | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: ATF6-related condition | ClinVar | PMID:28492532 | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 more ... | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 more ... | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 more ... | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26063662 | ATF6 | Human | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:24824130 and PMID:26063662 | ATF6 | Human | autoimmune interstitial lung, joint, and kidney disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autoimmune interstitial lung disease-arthritis syndrome | ClinVar | PMID:28492532 | ATF6 | Human | Charcot-Marie-Tooth disease type 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Charcot-Marie-Tooth disease and type I | ClinVar | PMID:28492532 | ATF6 | Human | fundus dystrophy | | IAGP | (Homo sapiens) and (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:25741868 and PMID:28492532 | ATF6 | Human | fundus dystrophy | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:25741868 | ATF6 | Human | fundus dystrophy | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:25741868 and PMID:30202406 | ATF6 | Human | gastrointestinal stromal tumor | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Gastrointestinal stromal tumor | ClinVar | PMID:28492532 | ATF6 | Human | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | ATF6 | Human | genetic disease | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | ATF6 | Human | genetic disease | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | ATF6 | Human | macular degeneration | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Macular dystrophy | ClinVar | PMID:28041643 | ATF6 | Human | parathyroid carcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Parathyroid carcinoma | ClinVar | PMID:28492532 | ATF6 | Human | sensorineural hearing loss | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Bilateral sensorineural hearing impairment | ClinVar | PMID:26029869 | ATF6 | Human | sensorineural hearing loss | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Bilateral sensorineural hearing impairment | ClinVar | PMID:25741868 more ... | |