Conditions
There are thousands of different genetic conditions that have been identified. This list includes just a few:
Conditions
- 22q11.2 Deletion Syndrome
- Abdominal Wall Defects
- Achondroplasia
- Apert Syndrome
- Becker Muscular Dystrophy
- Cartilage-Hair Hypoplasia
- CHARGE Syndrome
- Cleft lip/Cleft Palate
- Craniosynostosis
- Crouzon Syndrome
- Cystic Fibrosis
- Diastrophic Dysplasia
- Down Syndrome
- Duchenne Muscular Dystrophy
- Familial Combined Hyperlipidemia
- Ehlers-Danlos Syndrome
- Familial Hypercholesterolemia
- Familial Hyperlipoprotein(a)
- Familial Hypertriglyceridemia
- Familial Hypoalphalipoproteinemia
- Fragile X Syndrome
- Hereditary Hemochromatosis
- Homocystinuria
- Klinefelter Syndrome
- Marfan Syndrome
- Morquio Syndrome
- Myotonic Dystrophy, Type 1
- Neural Tube Defects (NTDs)
- Neurofibromatosis 1 (NF1)
- Neurofibromatosis 2 (NF2)
- Oculo-Auricular-Vertebral Spectrum
- Pfeiffer Syndrome
- Pierre Robin Sequence
- Schwannomatosis
- Smith-Lemli-Opitz Syndrome
- Spina Bifida
- Spondyloepiphyseal Dysplasia
- Treacher Collins Syndrome
- Trisomy X (Triple X syndrome)
- Trisomy 13
- Trisomy 18
- Turner Syndrome
- X-Linked Ichthyosis
- XYY Syndrome