Netzhauterkrankungen

Achromatopsie, ID 778.00 (6 Gene)

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autosomal-dominante Retinitis Pigmentosa (ADRP) - Basisdiagnostik, ID 770.00 (5 Gene)

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autosomal-rezessive Retinitis Pigmentosa (ARRP) - Basisdiagnostik, ID 771.00 (2 Gene)

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Bardet-Biedl-Syndrom (BBS), ID 780.00 (28 Gene)

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Bardet-Biedl-Syndrom (BBS) - Basisdiagnostik, ID 779.00 (10 Gene)

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Exsudative Vitreoretinopathie, ID 781.00 (6 Gene)

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Kongenitale stationäre Nachtblindheit (CSNB), ID 783.00 (16 Gene)

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Kongenitale stationäre Nachtblindheit (CSNB) - Basisdiagnostik, ID 782.00 (8 Gene)

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Lebersche kongenitale Amaurose (LCA), ID 766.00 (28 Gene)

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Lebersche kongenitale Amaurose (LCA) - Basisdiagnostik, ID 765.00 (8 Gene)

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Makula- und Netzhauterkrankungen - vollständiges Panel, ID 785.00 (197 Gene)

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Netzhautdystrophien - umfassende Diagnostik, ID 777.01 (158 Gene)

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Retinitis pigmentosa, ID 773.00 (90 Gene)

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sporadische Retinitis pigmentosa - Basisdiagnostik, ID 772.00 (6 Gene)

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Usher Syndrom - umfassende Diagnostik, ID 769.00 (15 Gene)

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Usher-Syndrom Typ 1 - Basisdiagnostik, ID 767.00 (4 Gene)

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Usher-Syndrom Typ 2 - Basisdiagnostik, ID 768.00 (1 Gene)

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Zapfen-Stäbchen-Dystrophie (ZSD), ID 775.00 (47 Gene)

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Zapfen-Stäbchen-Dystrophie (ZSD) - Basisdiagnostik, ID 774.00 (7 Gene)

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