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14 Cards in this Set
- Front
- Back
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Autosomal Dominant Diseases |
Achondroplasia ADPKD Familial Adenomatous polyposis Familial hypercholesterolemia Hereditary hemorrhagic telangiectasia Hereditary spherocytosis Huntington Disease Li-Fraumeni syndrome Marfan syndrome MEN NF1 NF2 Tuberous sclerosis von Hippel-Lindau disease |
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Autosomal Recessive Diseases |
Albinism ARPKD Cystic Fibrosis Glycogen storage diseases Hemochromatosis Kartgener syndrome Mucopolysaccharidosis (except Hunter syndrome) Phenylketonuria Sickle cell anemia Sphingolipidoses (except Fabry) Thalasemias Wilson Disease |
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X-Linked recessive |
Ornithine Transcarbamylase deficiency Fabry disease Wiskott-Aldrich syndrome Ocular albinism G6PD deficiency Hunter syndrome Bruton agammaglobulinemia Hemophilia A and B Lesch-Nyhan syndrome Duchenne and (Becker) muscular dystrophy |
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Oblivious Female Will Often Give Her Boys Her x-Linked Disorders |
Ornithine Transcarbamylase deficiency Fabry disease Wiskott-Aldrich syndrome Ocular albinism G6PD deficiency Hunter syndrome Bruton agammaglobulinemia Hemophilia A and B Lesch-Nyhan syndrome Duchenne and (Becker) muscular dystrophy |
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Oblivious |
Ornithine Transcarbamylase deficiency |
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Female |
Fabry disease |
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Will |
Wiskott-Aldrich syndrome |
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Often |
Ocular albinism |
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Give |
G6PD deficiency |
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Her |
Hunter syndrome |
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Boys |
Bruton agammaglobulinemia |
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Her |
Hemophilia A and B |
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x-Linked |
Lesch-Nyhan syndrome |
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Disorders |
Duchenne and (Becker) muscular dystrophy |
