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Clinical Disorder Search

Terms: night blindness, jaundice, cataracts, etc.
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Disorder Name Genes Alternate Names OMIM Inheritance
Usher Syndrome Type I MYO7A, CDH3, USH1C, PCDH15, USH1G retinitis pigmentosa and congenital deafness, USH1C, USH1D, USH1E, USH1F, USH1G, USH1H, USH1, USH1B (USH1A), USHiK 276900, 276904, 601067, 602083, 606943, 602097, 612632 autosomal recessive
Usher Syndrome Type II usherin, WHRN, GPR98 Usher syndrome type IIA, USH2A, USH2C, USH2D 276901, 605472, 611383 autosomal recessive
Usher Syndrome Type III CLRN1, HARS USH3 276902, 614504 autosomal recessive
Usher Syndrome Type IV ARSG USH4 618144 autosomal recessive