• Achromatopsia (DxOme Not Available) includes 6 Gene(s)

• Bardet–Biedl syndrome (BBS) (DxOme Not Available) includes 28 Gene(s)

• Bardet–Biedl syndrome (BBS) - common causes includes 26 Gene(s)

• Congenital stationary night blindness (CSNB) (DxOme Not Available) includes 16 Gene(s)

• Congenital stationary night blindness (CSNB) - common causes (DxOme Not Available) includes 8 Gene(s)

• Monogenic cone-rod (CORD) and macular dystrophies includes 62 Gene(s)

• Cone rod dystrophy (CRD) - common causes (DxOme Not Available) includes 7 Gene(s)

• Familial exudative vitreoretinopathy (FEVR) (DxOme Not Available) includes 7 Gene(s)

• Leber Congenital Amaurosis (LCA) – comprehensive panel (DxOme Not Available) includes 28 Gene(s)

• Leber Congenital Amaurosis (LCA) - common causes (DxOme Not Available) includes 8 Gene(s)

• Macular and Retinal diseases - complete panel (DxOme Not Available) includes 214 Gene(s)

• Retinal dystrophies - comprehensive panel includes 170 Gene(s)

• Retinitis pigmentosa – comprehensive panel (DxOme Not Available) includes 98 Gene(s)

• Autosomal dominant retinitis pigmentosa (ADRP) - common causes (DxOme Not Available) includes 6 Gene(s)

• Retinitis pigmentosa, sporadic - basic testing (DxOme Not Available) includes 7 Gene(s)

• Usher syndrome, type 1 - common causes (DxOme Not Available) includes 4 Gene(s)

• Usher syndrome, type 2 - common causes (DxOme Not Available) includes 1 Gene(s)

• Usher syndrome - comprehensive panel (DxOme Not Available) includes 15 Gene(s)