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ECLASS BASIC 14.0 (en)
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- 42 In-vitro diagnostic
- 42-06 Genetic testing (IVD)
- 42-06-01 Inborn gene or chromosome alteration
- 42-06-01-01 Cystic fibrosis (monogenetic, IVD)
- 42-06-01-02 Duchenne muscular dystrophy (monogenetic, IVD)
- 42-06-01-03 Factor V Leiden (monogenetic, IVD)
- 42-06-01-04 Fragile X Syndrome (monogenetic, IVD)
- 42-06-01-05 Haemochromatosis (monogenetic, IVD)
- 42-06-01-06 Haemophilia (monogenetic, IVD)
- 42-06-01-07 Huntington Chorea (monogenetic, IVD)
- 42-06-01-08 Polycystic kidney disease (monogenetic, IVD)
- 42-06-01-09 Sickle cell anemia (monogenetic, IVD)
- 42-06-01-10 Tay Sachs disease (monogenetic, IVD)
- 42-06-01-11 Thalassaemia (monogenetic, IVD)
- 42-06-01-12 Friedreich's ataxia (monogenetic, IVD)
- 42-06-01-13 Spinocerebellar ataxins type 1,2,3,6,7,8 (monogenetic, IVD)
- 42-06-01-14 Prothrombin mutation (monogenetic, IVD)
- 42-06-01-15 Alzheimer's disease (polygenetic, IVD)
- 42-06-01-16 Asthma (polygenetic, IVD)
- 42-06-01-17 Atherosclerosis (polygenetic, IVD)
- 42-06-01-18 Diabetes (polygenetic, IVD)
- 42-06-01-19 Hypertension (polygenetic, IVD)
- 42-06-01-20 Multiple sclerosis (polygenetic, IVD)
- 42-06-01-21 Osteoporosis (polygenetic, IVD)
- 42-06-01-22 Down's syndrome (chromosomal, IVD)
- 42-06-01-23 Edwards syndrome (chromosomal, IVD)
- 42-06-01-24 Klinefelter syndrome (chromosomal, IVD)
- 42-06-01-25 Pätau syndrome (chromosomal, IVD)
- 42-06-01-26 Turner syndrome (chromosomal, IVD)
- 42-06-01-27 HLA-Typing (polymorphism)
- 42-06-01-90 Inborn gene or chromosome alteration (unspecified)
Classification: 42060100 [ADU154003]
| Preferred name | 42-06-01 Inborn gene or chromosome alteration |
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| IRDI | 0173-1#01-ADU154#003 |
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