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No. ID Analyzed disease
181 197 Deep vein thrombosis / Peripheral arterial occlusive disease (PAOD) – F5 gene analysis (Leiden mutation), F2 gene analysis (G20210A mutation), MTHFR gene analysis – panel
182 198 Brachydactyly type B (genes ROR2 - exons 8 and 9, NOG - entire)
183 199 Symphalangism, proximal (GDF5, NOG genes)
184 200 FISH analysis with one centromere probe or X and Y chromosomes
185 201 FISH analysis with one specific probe
186 202 Karyotype from peripheral blood
187 203 Male infertility (CFTR gene – analysis of 7 mutations)
188 204 Cystic Fibrosis (CF) (36 mutations)
189 205 Cystic fibrosis (CF) (Carrier test for a known mutation)
190 206 Cystic Fibrosis (CF) (19 mutations)
191 207 Porphyria cutanea tarda
192 208 Muscular dystrophy, limb-girdle, type 1A
193 209 Hand – foot – genital syndrome
194 210 Fraser syndrome
195 211 Breast cancer, genetic predisposition - panel II (supplementary multi-gene test)
196 212 Breast cancer, genetic predisposition - panel I (multi-gene test)
197 213 Prostate cancer – genetic predisposition - panel (CHEK2 - 4 mutations, BRCA1, NBS1)
198 214 Colorectal cancer, genetic predisposition – panel (CHEK2, NOD2, P16)
199 215 Lung cancer – genetic predisposition - panel (NOD2, P16, P53 - 1 mutation, CYP1B1)
200 216 Ovarian cancer, genetic predisposition - panel (CHEK2, NOD2, CYP1B1)