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Index of genetic diseases offered by AC Gen Reading Life


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Disease/Phenotype Phenotype MIM number Gene Symbol Gene Name
Usher syndrome      
Usher syndrome, type 1B 276900 MYO7A  myosin VIIA
Usher syndrome, type 1C 276904 USH1C  Usher syndrome 1C (autosomal recessive, severe)
Usher syndrome, type 1D 601067 CDH23 cadherin-related 23
Usher syndrome, type 1D/F digenic 601067 CDH23 cadherin-related 23
Usher syndrome, type 1D/F digenic 601067 PCDH15  protocadherin-related 15
Usher syndrome, type 1F 602083 PCDH15  protocadherin-related 15
Usher syndrome, type 2A 276901 USH2A  Usher syndrome 2A (autosomal recessive, mild)
UV-induced skin damage 266300 MC1R  melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)

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