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Genetics
Inheritance Diseases
Question | Answer |
---|---|
Oculocutaneous albinism | AR |
ARPKD | AR |
Cystic fibrosis | AR |
Friedreich ataxia | AR |
glycogen storage diseases | AR |
hemochromatosis | AR |
Kartagener syndrome | AR |
mucopolysaccharidoses (except Hunter syndrome) | AR |
phenylketonuria | AR |
sickle cell anemia | AR |
Sphingolipidoses (except Fabry disease) | AR |
thalassemias | AR |
Wilson disease | AR |
Achondroplasia | AD |
ADPKD | AD |
familial adenomatous polyposis | AD |
familial adenomatous polyposis | AD |
hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) | AD |
hereditary spherocytosis | AD |
Huntington disease | AD |
Li-Fraumeni syndrome | AD |
Marfan syndrome | AD |
multiple endocrine neoplasias | AD |
myotonic muscular dystrophy | AD |
neurofibromatosis type 1 (von Recklinghausen disease) | AD |
neurofibromatosis type 2 | AD |
tuberous sclerosis | AD |
Von Hippel-Lindau disease | AD |
Ornithine transcarbamylase deficiency | X-linked recessive |
Fabry disease | X-linked recessive |
Wiskott-Aldrich syndrome | X-linked recessive |
Ocular albinism | X-linked recessive |
G6PD deficiency | X-linked recessive |
Hunter syndrome | X-linked recessive |
Bruton agammaglobulinemia | X-linked recessive |
Hemophilia A and B | X-linked recessive |
Lesch-Nyhan syndrome | X-linked recessive |
Duchenne (and Becker) muscular dystrophy. | X-linked recessive |