Disorders: U
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| Disorders | Alternate Names | Genes | Inheritance Pattern |
|---|---|---|---|
| Usher Syndrome Type I | retinitis pigmentosa and congenital deafness, USH1, USH1B (USH1A), USH1C, USH1D, USH1E, USH1F, USH1G, USH1H, USHiK | CDH3, MYO7A, PCDH15, USH1C, USH1G | autosomal recessive |
| Usher Syndrome Type II | USH2A, USH2C, USH2D, Usher syndrome type IIA | GPR98, usherin, WHRN | autosomal recessive |
| Usher Syndrome Type III | USH3 | CLRN1, HARS | autosomal recessive |
| Usher Syndrome Type IV | USH4 | ARSG | autosomal recessive |