CentoVision panel (378 gena) je pažljivo dizajniran da bi se otkrili genetski uzroci bolesti oka, uključujući i one koji dovode do sljepila kod novorođenčadi, djece i odraslih. Podrazumijeva najčešće oftalmološke bolesti kao što su, urođeni glaukom, retinitis pigmentosa, strgardt - ova bolest, Stickler sindrom, ahromatopsija i Usher sindrom. Takođe ispituje i različite tipove albinizma.
Achromatopsia panel
Albinism panel
Bardet-Biedl panel
Cataract panel
Cone-rod and cone dystrophy panel
Flecked retina panel
Glaucoma panel
Hermansky-Pudlak syndrome panel
Leber congenital amaurosis panel
Meckel syndrome panel
Microphthalmia/anophthalmia/coloboma spectrum panel
Oculomotor apraxia panel
Ophthalmoplegia progressive external panel
Optic atrophy panel
Retinitis pigmentosa panel, autosomal dominant
Retinitis pigmentosa panel, autosomal recessive
Stargardt disease panel
Stickler syndrome panel
Usher syndrome panel
Vitreoretinopathy and Wagner syndrome panel
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