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 ... 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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 ... 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