Tumorerkrankungen
Tumorerkrankungen


000.00 Schwannomatose I SMARCB1, LZTR1

000.00 Neurofibromatose I NF1

000.00 Exostosis multiplex I EXT1, EXT2

000.00 Leiomyomatose I FH

000.00 Gorlin-Syndrom I PTCH1, SUFU

000.00 Tuberöse Sklerose I TSC1, TSC2

093.01 Erbliche Tumorerkrankungen – umfassende DiagnostikACD, AIP, AKT1, ALK, APC, ATM, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, BUB1B, CASR, CBL, CDC73, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A, CDKN2B, CEP57, CFTR, CHEK2, CTNNA1, CTRC, DICER1, DIS3L2, EPCAM, EZH2, FAN1, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, FH, FLCN, GNAS, GPC3, GPC4, GREM1, HOXB13, KIT, LZTR1, MAP2K1, MAP2K2, MAX, MDH2, MEN1, MET, MITF, MLH1, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NRAS, NSD1, NTHL1, PALB2, PDGFRA, PHOX2B, PIK3CA, PMS1, PMS2, POLD1, POLE, POT1, PRKAR1A, PRSS1, PTCH1, PTCH2, PTEN, PTPN11, RAD50, RAD51C, RAD51D, RAF1, RB1, RECQL4, RET, RNF43, RUNX1, SDHA, SDHAF2, SDHB, SDHC, SDHD, SEC23B, SHOC2, SLX4, SMAD4, SMARCA4, SMARCB1, SMARCE1, SOS1, SPINK1, SPRED1, STK11, SUFU, TERF2IP, TERT, TMEM127, TP53, TSC1, TSC2, VHL, WT1, XRCC2 | Panel > 25 kB