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Autosomal-Dominant Diseases.

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Adult polycystic kidney disease.


Familial hyperchloresterolemia (type IIA).
Marfan's syndrome.
Von Recklinghausen's disease (NFT1).
Von Hippel-Lindau disease.
Huntington's disease.
Familial Adenomatous Polyposis.
Hereditary Sperocytosis.

Autosomal Recessive Diseases.


1. CF.
2. albinism.
3. alpha 1 antitrypsin deficiency.
4. phenylketonuria.
5. thalassemias.
6. sicke cell anemia.
7. glycogen storage diseases.
8. mucopolysaccharidoses (except
Hunter's).
9. sphingolipidoses (except Fabry's).
10.infant polycystic kidney disease.
11. hemochromatosis.