Monogenetic disorders
W01060101 274 devices
Subcategories
- W0106010101 Cystic fibrosis
- W0106010102 Duchenne muscular dystrophy
- W0106010103 Factor V leiden
- W0106010104 Fragile X syndrome
- W0106010105 Haemochromatosis
- W0106010106 Haemophilia
- W0106010107 Huntington chorea
- W0106010108 Polycystic kidney disease
- W0106010109 Sickle cell anemia
- W0106010110 Tay sachs disease
- W0106010111 Thalassaemia
- W0106010112 Friedreich's ataxia
- W0106010113 Spinocerebellar ataxins type 1,2,3,6,7,8
- W0106010114 Prothrombin mutation
- W0106010115 Combined factor II / factor V leiden
- W0106010116 Other thrombophilia mutations (proc, pros1, mthfr, serpinc1, sepine1, f11, f12, f13, other f2/f5)
- W0106010117 Other hemophilia mutations (vwf, f8, f9)
- W0106010118 Myotonic dystrophy type 1 or steinert's disease
- W0106010199 Monogenetic disorders tests - other