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Inheritance of Dz
Pathology S2
| Disease | Inheritance |
|---|---|
| Huntington Dz | AD |
| Neurofibromatosis | AD |
| Myotonic Dystrophy | AD |
| Tuberous Sclerosis | AD |
| Polycystic Kidney Dz | AD |
| Wilm's Tumor | AD |
| Familial Polyposis Coli | AD |
| Marfan's | AD |
| Ehlers Danlos (some) | AD |
| Osteogenesis Imperfected (I-IV) | AD |
| Achondroplasia | AD |
| Familial Hypercholesterolemia | AD |
| Acute Intermittent Porphyria | AD |
| Hereditary Spherocytosis | AD |
| Vov willebrand's | AD |
| Cystic Fibrosis | AR |
| PKU | AR |
| Galactosemia | AR |
| Homocystinuria | AR |
| Lysosomal Storage Dzs | AR |
| alpha-1 antitrypsin deficiency | AR |
| Wilson's | AR |
| Hemochromatosis | AR |
| Glycogen Storage Dzs | AR |
| Sickle cell | AR |
| Thalassemia | AR |
| Ehlers Danlos (some) | AR |
| Alkaptonuria | AR |
| Osteogenesis Imperfecta Type II | AR |
| Friedreich Ataxia | AR |
| Albinism | AR |
| Fabry's Dz | XR |
| Hunter's Syndrome | XR |
| Lesch-Nyhan Syndrome | XR |
| Diabetes Insipidus | XR |
| Hemophilia A | XR |
| Hemophilia B | XR |
| G6PD Deficiency | XR |
| Fragile X Syndrome | XR |
| Vitamin D Resistant Rickets | XD |