Neuropathien / Motoneuronerkrankungen

Amyotrophe Lateralsklerose, familiär, ID 019.03 (32 Gene)

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Amyotrophe Lateralsklerose, familiär - Basisdiagnostik, ID 263.02 (15 Gene)

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Analgesie, angeborene Schmerzunempfindlichkeit, ID 753.00 (3 Gene)

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Andermannsyndrom (SLC12A6) (1 Gene)

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Congenital Cataracts, Facial Dysmorphism, and Neuropathy (CCFDN), CTDP1 c.863+389C>T (1 Gene)

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Differentialdiagnosen zur SMA des Erwachsenenalters, ID 262.00 (9 Gene)

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Differentialdiagnosen zur SMA des Säuglings, ID 261.00 (5 Gene)

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Hereditäre neuralgische Amyotrophie / HNA (SEPT9) (1 Gene)

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Neuropathie PMP22-Dosistestung (1 Gene)

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Neuropathie PMP22-Sequenzierung (1 Gene)

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Neuropathie, motorisch /dHMN - Basisdiagnostik, ID 258.01 (12 Gene)

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Neuropathie, motorisch-sensibel / CMT1, CMT2, dHMN - umfassende Diagnostik, ID 288.02 (117 Gene)

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Neuropathie, motorisch-sensibel, axonal / CMT2 - Basisdiagnostik, ID 287.03 (11 Gene)

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Neuropathie, motorisch-sensibel, demyelinisierend / CMT1 - Basisdiagnostik, ID 286.01 (14 Gene)

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Neuropathie, Natriumkanal-assoziiert, ID 289.00 (3 Gene)

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Neuropathie, sensorisch (autonom) - HS(A)N, ID 015.02 (25 Gene)

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Neuropathie, sensorisch - Familiäre Dysautonomie / HSAN3 und HSAN4 , ID 260.00 (2 Gene)

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Neuropathie, sensorisch / HSAN1 und HSAN2 , ID 259.00 (10 Gene)

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Neuropathie/Motoneuropathie - Gesamtpanel, ID 086.05 (279 Gene)

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Schmerzhafte-sensibel betonte PNP, ID 845.00 (11 Gene)

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SMARD1 (IGHMBP2) (1 Gene)

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SORD-assoziierte Neuropathie (1 Gene)

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Spinale Muskelatrophie (SMA 5q), MLPA (1 Gene)

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Spinobulbäre Muskelatrophie (SBMA, Kennedy), AR-Repeat (1 Gene)

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Transthyretin-Amyloid-Neuropathie (TTR) (1 Gene)

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