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ECLASS BASIC 14.0 (de)
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- 42 In-vitro Diagnostik
- 42-06 Gentest (IVD)
- 42-06-01 Angeborene Gen- und Chromosomveränderung
- 42-06-01-01 Zystische Fibrose (Monogenetisch, IVD)
- 42-06-01-02 Duchenne Muskeldystrophie (Monogenetisch, IVD)
- 42-06-01-03 Faktor- V- Leiden (Monogenetisch, IVD)
- 42-06-01-04 Fragiles X Syndrom (Monogenetisch, IVD)
- 42-06-01-05 Hämochromatose (Monogenetisch, IVD)
- 42-06-01-06 Hämophilie (Monogenetisch, IVD)
- 42-06-01-07 Chorea Huntington (Monogenetisch, IVD)
- 42-06-01-08 Polyzystische Nierenkrankheit (Monogenetisch, IVD)
- 42-06-01-09 Sichelzellenanämie (Monogenetisch, IVD)
- 42-06-01-10 Tay Sachs Krankheit (Monogenetisch, IVD)
- 42-06-01-11 Thalassämie (Monogenetisch, IVD)
- 42-06-01-12 Friedreich's Ataxie (Monogenetisch, IVD)
- 42-06-01-13 Spinozerebelläre Ataxien Typ 1,2,3,6,7,8 (Monogenetisch, IVD)
- 42-06-01-14 Prothrombinmutation (Monogenetisch, IVD)
- 42-06-01-15 Alzheimer Krankheit (Polygenetisch, IVD)
- 42-06-01-16 Asthma (Polygenetisch, IVD)
- 42-06-01-17 Atherosklerose (Polygenetisch, IVD)
- 42-06-01-18 Diabetes (Polygenetisch, IVD)
- 42-06-01-19 Hypertonie (Polygenetisch, IVD)
- 42-06-01-20 Multiple Sklerose (Polygenetisch, IVD)
- 42-06-01-21 Osteoporosis (Polygenetisch, IVD)
- 42-06-01-22 Down-Syndrom (Chromosomal, IVD)
- 42-06-01-23 Edwards-Syndrom (chromosomal, IVD)
- 42-06-01-24 Klinefelter- Syndrom (chromosomal, IVD)
- 42-06-01-25 Pätau-Syndrom (chromosomal, IVD)
- 42-06-01-26 Turner-Syndrom (chromosomal, IVD)
- 42-06-01-27 HLA-Typisierung (Polymorphismus)
- 42-06-01-90 Angeborene Gen- und Chromosomveränderung (nicht spezifiziert)
Classification: 42060100 [ADU154003]
Preferred name | 42-06-01 Angeborene Gen- und Chromosomveränderung |
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IRDI | 0173-1#01-ADU154#003 |
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