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) |