Herzerkrankungen

Actionable Gene-Herz-Gefäßerkrankungen, ID 864.01 (36 Gene)

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Angeborene Herzfehler - Gesamtpanel, ID 185.02 (50 Gene)

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Arrhythmogene Erkrankungen - umfassende Diagnostik, ID 181.02 (44 Gene)

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Arrhythmogene Kardiomyopathie (ACM), ID 179.03 (12 Gene)

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Arterielle Hypertonie, monogen, ID 999.01 (16 Gene)

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Barth-Syndrom (TAZ) (1 Gene)

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Brugada-Syndrom, ID 865.01 (12 Gene)

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Catecholaminerge polymorphe ventrikuläre Tachykardie (CPVT), ID 180.02 (6 Gene)

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Danon-Disease (LAMP2) (1 Gene)

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DiGeorge-Syndrom, Mikrodeletion 22q11.2, MLPA (1 Gene)

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Herzerkrankungen - Gesamtpanel, ID 186.04 (198 Gene)

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Kardiomyopathie, dilatativ, ID 073.04 (32 Gene)

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Kardiomyopathie, hypertrophisch, ID 072.03 (23 Gene)

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Kardiomyopathien, umfassende Diagnostik, ID 088.05 (169 Gene)

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Karyotypisierung (konventionelle Chromosomenanalyse) (1 Gene)

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Long-QT-Syndrom (LQTS), ID 132.02 (17 Gene)

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Marfan-Syndrom, ID 715.00 (1 Gene)

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Marfan-Syndrom Differentialdiagnosen, ID 957.00 (8 Gene)

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Microarray (hochauflösende Chromosomenanalyse) (1 Gene)

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Morbus Fabry I GLA, ID 977.00 (1 Gene)

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mtDNA-Komplettsequenzierung (1 Gene)

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Non-compaction Kardiomyopathie (NCCM), ID 928.00 (7 Gene)

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Noonan-Syndrom - PTPN11 Gen, ID 159.01 (1 Gene)

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Noonan-Syndrom, weitere Gene, ID 285.03 (12 Gene)

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Phelan-Mcdermid-Syndrom, Mikrodeletion 22q13.3, MLPA (1 Gene)

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Plötzlicher Herztod_Basisdiagnostik, ID 863.01 (4 Gene)

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Rasopathien, ID 160.05 (22 Gene)

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Short-QT-Syndrom, ID 739.02 (7 Gene)

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Transthyretin-Amyloidose I TTR, ID 979.00 (1 Gene)

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Williams-Beuren-Syndrom, Mikrodeletion 7q11.23, MLPA (1 Gene)

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