Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | atypical Gaucher's disease due to saposin C deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Gaucher disease more ... | ClinVar | PMID:25741868 | atypical Gaucher's disease due to saposin C deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Gaucher disease more ... | ClinVar | | Atypical Krabbe Disease due to Saposin A Deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Krabbe disease more ... | ClinVar | PMID:25741868 | Atypical Krabbe Disease due to Saposin A Deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Krabbe disease more ... | ClinVar | | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:11138009 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:26467025, PMID:28492532 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:15660226 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:21436283 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:22135276 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:23804846 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:11138009 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:21940737 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:22135276 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043, PMID:24033266 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266, PMID:26467025 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:22607986 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:22135276 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:21569298 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:11090341 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:22899989 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:25279224 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:16679490 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:28492532 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:19888295, PMID:28492532 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266, PMID:28492532 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:21569298 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:25741868, PMID:28492532 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:17850630, PMID:22899989 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:11857743 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:23804846 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:16679490 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:12075507 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:19888295 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:20146813 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:18429043 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:15660226 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:22899989 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:25741868 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:24033266, PMID:25741868 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:16679490 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:21940737 more ... | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness, autosomal recessive 12 | ClinVar | PMID:25963016 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601386 | ClinVar | PMID:12522556 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601386 | ClinVar | PMID:11090341 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601386 | ClinVar | PMID:12910270, PMID:15829536 | autosomal recessive nonsyndromic deafness 12 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601386 | ClinVar | PMID:24033266 | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PROSAPOSIN DEFICIENCY | ClinVar | PMID:25741868 | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Sphingolipid activator protein 1 deficiency | ClinVar | PMID:24033266 more ... | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Combined saposin deficiency | ClinVar | PMID:24033266, PMID:28492532 | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Combined saposin deficiency | ClinVar | PMID:18429043 more ... | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Combined saposin deficiency | ClinVar | PMID:24033266, PMID:25741868 | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Combined saposin deficiency | ClinVar | PMID:24033266 | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PROSAPOSIN DEFICIENCY | ClinVar | PMID:18429043 more ... | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Combined saposin deficiency | ClinVar | PMID:25991456 | combined saposin deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PROSAPOSIN DEFICIENCY | ClinVar | | Deafness | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Deafness | ClinVar | | fundus dystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | | fundus dystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:11138009 more ... | fundus dystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:11138009 more ... | fundus dystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:30718709 | fundus dystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:28492532 | fundus dystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:24033266, PMID:28492532 | fundus dystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:24033266 | fundus dystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinal dystrophy | ClinVar | PMID:18429043, PMID:28492532 | genetic disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:12075507 more ... | genetic disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:24033266 more ... | genetic disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:12075507 more ... | genetic disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:27743452, PMID:28492532 | Hearing Loss | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive | ClinVar | | Hearing Loss | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Hearing loss | ClinVar | PMID:28492532 | Hearing Loss | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive | ClinVar | PMID:24033266, PMID:28492532 | Hearing Loss | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive | ClinVar | PMID:25741868 | Hearing Loss | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive | ClinVar | PMID:24033266, PMID:25741868 | Hearing Loss | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive | ClinVar | PMID:24033266 | Hearing Loss | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive | ClinVar | PMID:18429043 more ... | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Leukodystrophy, Globoid Cell | ClinVar | PMID:25741868 | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency | ClinVar | PMID:24033266 more ... | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency | ClinVar | PMID:24033266, PMID:28492532 | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency | ClinVar | PMID:18429043 more ... | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency | ClinVar | PMID:24033266, PMID:25741868 | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency | ClinVar | PMID:24033266 | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Leukodystrophy, Globoid Cell | ClinVar | PMID:18429043 more ... | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Galactosylceramide beta-galactosidase deficiency | ClinVar | PMID:25991456 | Krabbe disease | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Leukodystrophy, Globoid Cell | ClinVar | | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Arylsulfatase A Deficiency | ClinVar | PMID:25741868 | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Metachromatic leukodystrophy | ClinVar | PMID:24033266 more ... | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Metachromatic leukodystrophy | ClinVar | PMID:24033266, PMID:28492532 | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Metachromatic leukodystrophy | ClinVar | PMID:18429043 more ... | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Metachromatic leukodystrophy | ClinVar | PMID:24033266, PMID:25741868 | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Metachromatic leukodystrophy | ClinVar | PMID:24033266 | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Arylsulfatase A Deficiency | ClinVar | PMID:18429043 more ... | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Metachromatic leukodystrophy | ClinVar | PMID:25991456 | metachromatic leukodystrophy | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Arylsulfatase A Deficiency | ClinVar | | Metachromatic Leukodystrophy due to Saposin B Deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Saposin B Deficiency | ClinVar | PMID:25741868 | Metachromatic Leukodystrophy due to Saposin B Deficiency | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Saposin B Deficiency | ClinVar | | Neurodevelopmental Disorders | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Neurodevelopmental abnormality | ClinVar | | Neurodevelopmental Disorders | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Neurodevelopmental abnormality | ClinVar | PMID:12075507 more ... | nonsyndromic deafness | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic hearing loss and deafness | ClinVar | PMID:28492532 | nonsyndromic deafness | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic hearing loss and deafness | ClinVar | PMID:17850630 more ... | nonsyndromic deafness | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic hearing loss and deafness | ClinVar | PMID:18429043 more ... | nonsyndromic deafness | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic hearing loss and deafness | ClinVar | PMID:24033266 more ... | nonsyndromic deafness | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Nonsyndromic hearing loss and deafness | ClinVar | PMID:24033266 | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:25741868 | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:11138009 more ... | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:25741868, PMID:28492532 | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:21436283 more ... | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:16679490 more ... | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:24033266 more ... | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:11857743 more ... | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:16679490 more ... | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:24033266 more ... | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:28413019, PMID:28492532 | pituitary adenoma 5 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: PITUITARY ADENOMA 5, MULTIPLE TYPES | ClinVar | PMID:28413019 | retinitis pigmentosa | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar | PMID:30718709 | retinitis pigmentosa | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar | PMID:24033266 more ... | retinitis pigmentosa | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar | PMID:18429043 more ... | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | PMID:24033266, PMID:25741868 | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | PMID:28492532 | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | PMID:24033266, PMID:28492532 | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | PMID:12075507 more ... | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | PMID:18429043 more ... | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | PMID:18429043 more ... | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | PMID:25741868 | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | | retinitis pigmentosa-deafness syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa-deafness syndrome | ClinVar | PMID:24033266 | sensorineural hearing loss | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: sensorineural hearing loss disorder | ClinVar | PMID:22899989 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:24033266 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:24033266 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:11138009 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:11138009 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:24033266 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:18429043 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:22135276, PMID:24033266 | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:25991456 | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:11857743 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:28492532 | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:17850630 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:21940737 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:12075507 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:15537665 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:24033266 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Hallgren syndrome | ClinVar | PMID:12075507 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:24033266 | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Hallgren syndrome | ClinVar | PMID:18429043 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Hallgren syndrome | ClinVar | PMID:18429043 more ... | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:24033266, PMID:26681316 | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Hallgren syndrome | ClinVar | PMID:25741868 | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Hallgren syndrome | ClinVar | | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Hallgren syndrome | ClinVar | PMID:24033266, PMID:28492532 | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Hallgren syndrome | ClinVar | PMID:24033266, PMID:25741868 | Usher syndrome | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:24033266 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1 | ClinVar | PMID:15537665 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:11138009 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:26467025, PMID:28492532 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:21436283 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:11138009 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:22135276 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266, PMID:25963016 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266, PMID:25741868 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:22607986 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:20146813 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:18429043 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:17850630 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:21569298 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:17850630 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:23804846 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:18429043 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:18429043 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:23804846, PMID:24033266 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:18429043, PMID:24033266 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:18429043 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:28413019, PMID:28492532 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266, PMID:26467025 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:16679490 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:22135276, PMID:24033266 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:18429043 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:21569298 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:11857743 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12522556 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:17850630 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266, PMID:27792758 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:25991456 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:18429043 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:21940737 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:17850630 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:21940737 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:28492532, PMID:29148562 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:24033266, PMID:28492532 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1 | ClinVar | PMID:25741868, PMID:28492532 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1 | ClinVar | PMID:25741868 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:21569298 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1 | ClinVar | | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1 | ClinVar | PMID:12075507 more ... | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1 | ClinVar | PMID:28492532 | Usher syndrome type 1 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1 | ClinVar | PMID:12075507, PMID:15537665 | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:24033266, PMID:28492532 | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:24033266 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:11138009 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:18429043 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:24033266 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:18429043 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:22135276, PMID:24033266 | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:11857743 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:25991456 | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:11138009 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:24033266, PMID:25741868 | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:28492532 | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:18429043 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:24033266 | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:24033266 more ... | Usher Syndrome Type 1B | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness | ClinVar | PMID:21940737 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:21940737 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:26467025, PMID:28492532 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:11138009 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:15660226 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:21436283 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:25741868, PMID:28492532 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:20146813 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:22135276 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:16679490 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:22899989 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:23804846 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:22135276 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:22607986 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:11138009 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1D | ClinVar | PMID:24033266, PMID:28492532 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:22135276 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043, PMID:24033266 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:21569298 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:16679490 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266, PMID:26467025 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:28492532 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:11138009 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:21569298 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17850630 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1D | ClinVar | PMID:12075507 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:11857743 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:23804846 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:16679490 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1D | ClinVar | PMID:25741868 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:24033266 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:18429043 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:15660226 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:17407589, PMID:28492532 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:11138009 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: USHER SYNDROME, TYPE ID | ClinVar | PMID:24033266, PMID:25741868 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 1D | ClinVar | PMID:21940737 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome, type 1D | ClinVar | PMID:16679490 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by null | ClinVar | PMID:12075507, PMID:15537665 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601067 | ClinVar | PMID:25991456 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601067 | ClinVar | PMID:11138009 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601067 | ClinVar | PMID:11090341 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601067 | ClinVar | PMID:11138009 more ... | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601067 | ClinVar | PMID:24033266 | Usher syndrome type 1D | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by OMIM:601067 | ClinVar | | Usher syndrome type 2 | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: Usher syndrome type 2 | ClinVar | PMID:25741868 | Usher syndrome type 2A | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: USHER SYNDROME, TYPE IIA | ClinVar | PMID:12075507 more ... | Usher Syndrome, Type ID/F | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: USHER SYNDROME more ... | ClinVar | PMID:15537665 more ... | Usher Syndrome, Type ID/F | | ISO | RGD:733851 | 8554872 | ClinVar Annotator: match by term: USHER SYNDROME more ... | ClinVar | PMID:12075507, PMID:15537665 | |
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Imported Disease Annotations - CTD
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References
References - curated
| 1. | Boeda B, etal., EMBO J 2002 Dec 16;21(24):6689-99. |
| 2. | Di Palma F, etal., Gene 2001 Dec 27;281(1-2):31-41. |
| 3. | Di Palma F, etal., Nat Genet. 2001 Jan;27(1):103-7. |
| 4. | Gillespie PG and Muller U, Cell. 2009 Oct 2;139(1):33-44. doi: 10.1016/j.cell.2009.09.010. |
| 5. | Hwang JH, etal., Otolaryngol Head Neck Surg. 2012 Sep;147(3):531-4. doi: 10.1177/0194599812446904. Epub 2012 May 11. |
| 6. | Kawai J, etal., Nature. 2001 Feb 8;409(6821):685-90. |
| 7. | Kazmierczak P and Muller U, Trends Neurosci. 2012 Apr;35(4):220-9. doi: 10.1016/j.tins.2011.10.007. Epub 2011 Dec 15. |
| 8. | Libby RT, etal., Exp Eye Res. 2003 Dec;77(6):731-9. |
| 9. | MGD data from the GO Consortium |
| 10. | MGD IEA |
| 11. | Noben-Trauth K, etal., Nat Genet 2003 Sep;35(1):21-3. Epub 2003 Aug 10. |
| 12. | Okazaki Y, etal., Nature. 2002 Dec 5;420(6915):563-73. |
| 13. | OMIM Disease Annotation Pipeline |
| 14. | Reiners J, etal., Invest Ophthalmol Vis Sci 2003 Nov;44(11):5006-15. |
| 15. | RGD automated import pipeline |
| 16. | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
| 17. | RGD automated import pipeline for gene-chemical interactions |
| 18. | Wagatsuma M, etal., Clin Genet. 2007 Oct;72(4):339-44. |
| 19. | Wright AF, etal., Nat Rev Genet. 2010 Apr;11(4):273-84. doi: 10.1038/nrg2717. |
| 20. | Yang M, etal., Wei Sheng Yan Jiu. 2006 Jan;35(1):19-22. |
Additional References at PubMed
| PMID:544312 | PMID:678292 | PMID:1912584 | PMID:5098070 | PMID:5955164 | PMID:7333462 | PMID:7610888 | PMID:8034315 | PMID:8735078 | PMID:8790740 | PMID:9021139 | PMID:9039475 |
| PMID:9325047 | PMID:9447922 | PMID:9641316 | PMID:10349636 | PMID:10452381 | PMID:10535453 | PMID:10984423 | PMID:11042159 | PMID:11076861 | PMID:11090341 | PMID:11112345 | PMID:11138009 |
| PMID:11175788 | PMID:11322776 | PMID:11335078 | PMID:11350126 | PMID:11386759 | PMID:11423214 | PMID:11678164 | PMID:12121736 | PMID:12204345 | PMID:12209292 | PMID:12407180 | PMID:12787792 |
| PMID:13336002 | PMID:13853422 | PMID:14648237 | PMID:14759567 | PMID:15057245 | PMID:15276680 | PMID:15537665 | PMID:15572405 | PMID:15590703 | PMID:15692809 | PMID:15820310 | PMID:15882573 |
| PMID:15882574 | PMID:15925194 | PMID:15928608 | PMID:16005171 | PMID:16141072 | PMID:16141073 | PMID:16219682 | PMID:16235133 | PMID:16281288 | PMID:16426780 | PMID:16481439 | PMID:16545802 |
| PMID:16579977 | PMID:16897347 | PMID:16962269 | PMID:17050716 | PMID:17175124 | PMID:17329413 | PMID:17360538 | PMID:17567809 | PMID:17805295 | PMID:17967520 | PMID:18001149 | PMID:18280008 |
| PMID:18339676 | PMID:18662770 | PMID:18799693 | PMID:18971469 | PMID:18996172 | PMID:19057657 | PMID:19270079 | PMID:19321743 | PMID:19339464 | PMID:19487694 | PMID:19756182 | PMID:20058854 |
| PMID:20095043 | PMID:20332152 | PMID:20399731 | PMID:20470874 | PMID:20498078 | PMID:20505086 | PMID:20628639 | PMID:20639393 | PMID:20644563 | PMID:20739546 | PMID:20799038 | PMID:20976199 |
| PMID:21165971 | PMID:21211561 | PMID:21267068 | PMID:21272629 | PMID:21423608 | PMID:21436032 | PMID:21532990 | PMID:21677750 | PMID:21689626 | PMID:21865467 | PMID:21873635 | PMID:21875659 |
| PMID:22138310 | PMID:22238076 | PMID:22326520 | PMID:22363448 | PMID:22381527 | PMID:22787034 | PMID:22952717 | PMID:23135401 | PMID:23217710 | PMID:23359017 | PMID:23384607 | PMID:23592719 |
| PMID:23658152 | PMID:23792079 | PMID:24172198 | PMID:24221507 | PMID:24239741 | PMID:24920589 | PMID:24952961 | PMID:25624266 | PMID:25762674 | PMID:25852546 | PMID:25904789 | PMID:25921334 |
| PMID:26620972 | PMID:26748055 | PMID:26876963 | PMID:26936824 | PMID:27255811 | PMID:27349180 | PMID:27882946 | PMID:28287619 | PMID:28345280 | PMID:28705869 | PMID:28818524 | PMID:28891466 |
| PMID:29111324 | PMID:29261728 | PMID:29486248 | PMID:29874579 | PMID:30033219 | PMID:30597229 | PMID:31247458 | PMID:31776257 | PMID:31818953 | PMID:31949136 | PMID:32003747 | PMID:32327469 |
| PMID:32514013 | PMID:32987832 | PMID:33009420 |
Genomics
