Tumorerkrankungen

Basalzell-Naevus-Syndrom (Gorlin-Syndrom), ID 806.00 (3 Gene)

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CUP - Cancer of unknown primary, ID 847.00 (8 Gene)

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Erbliche Tumorerkrankungen, umfassende Diagnostik, ID 093.02 (123 Gene)

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Exostosis multiplex (EXT1, EXT2) (1 Gene)

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FLCN Birt-Hogg-Dube Syndrom (1 Gene)

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Gorlin-Syndrom (PTCH1, SUFU, PTCH2) (3 Gene)

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Leiomyomatose (FH) (1 Gene)

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LiFraumeni-Syndrom (TP53, CHEK2) (2 Gene)

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Malignes Melanom, ID 705.00 (9 Gene)

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Neurofibromatose / Schwannomatose, ID 704.00 (5 Gene)

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PreCan, ID 921.00 (70 Gene)

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PreCan+, ID 935.00 (70 Gene)

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Tuberöse Sklerose, ID 805.00 (2 Gene)

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