Achondroplasia |
Marfan Syndrom |
Alkaptonuria |
Neurofibrmatosis |
Cystic Fibrosis |
Oculocutaneous Albinism (Type I or II) |
Ehlers - Danols Syndrome Classica (Thype I or II) |
Osteogenesis Imperfecta |
Fragile X Syndrome |
Progeria |
Hemophilia A |
Sickle Cell Disease |
Huntington's Disease |
Tay-Sachs Disease |
Klinefelter Syndrome |
Trisomy 21 |
Lou Gehrig's Disease (ALS) |
Trisomy X |
Color Blindness |
Turner's Syndrome |