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Metabolic disease caused by inability to breakdown the amino acid phenylalanine. |
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Inability to produce pigment melanin |
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Definition
A blood protein which is inherited as a dominant trait and can cause erythroblastosis fetalis. |
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Gene expression is different in males & females, Ex: baldness |
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Definition
X-linked trait that affects 8% of male population, lack of vision protein--opsins. |
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Most frequent genetic disease found among individuals of African descent, 1 in 12 carrier. |
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Definition
Inheritance pattern of roan shorthorn cattle and of pink 4 o'clocks. |
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Definition
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X-linked trait known as "Bubble Boy" Disease, males lack T and/or B lymphocytes. |
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The only viable human monosomy |
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Free-bleeders disease, X-linked |
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Definition
Type of inheritance expressed by A & B of the A,B,O blood group antigens |
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Definition
Hemochromatosis, 1 in 8 is a carrier, 1 in 200 affected |
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Definition
Typically expressed in only 1 sex, Ex: beard growth |
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Definition
Excess production of mucus by exocrine glands |
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