Heredity Flashcards

1
Q

Picture of chromosome arranged in pairs

A

Karyotype

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2
Q

Two of the 46 chromosomes

A

Sex chromosomes

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3
Q

XY

A

Males

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4
Q

XX

A

Females

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5
Q

The remaining 44 chromosomes

A

Autosomes

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6
Q

Full set of genetic information on DNA

A

Genome

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7
Q

A chart that shows how a human trait is transmitted through through different family generations

A

Pedigree

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8
Q

Several genes are responsible for blood groups but the best known are the ABO blood groups and Rh blood group

A

Blood Group Genes

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9
Q

Rh+

A

Dominant

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10
Q

Rh-

A

Recessive

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11
Q

a rare inherited metabolic disorder that affects the body’s ability to break down the amino acid phenylalanine

A

PKU

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12
Q

results in a nervous system breakdown and early death

A

Tay-Sachs

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13
Q

Lack of skin pigmentation (autosomal recessive)

A

Albino

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14
Q

a genetic disease that causes thick mucus to build up in the body, leading to breathing and digestion problems.

A

Cystic Fibrosis

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15
Q

Form of dwarfism

A

Achondroplasia

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16
Q

Caused by a dominant allele for a protein found in brain cells

A

Huntington’s Disease

17
Q

an inherited blood disorder that causes abnormal red blood cells

A

Sickle Cell Disease

18
Q

Located on the x or y chromosome. Most sex-linked genes are found on the x chromosome

A

Sex-linked genes

19
Q

Inability to distinguish certain colors

A

Colorblindness

20
Q

a rare, inherited bleeding disorder that prevents blood from clotting properly

A

Hemophilia

21
Q

Progressive weakening and loss of skeletal muscle

A

Duchenne Muscular Dystrophy

22
Q

a process that silences one of the two X chromosomes in female mammals

A

X chromosome inactivation

23
Q

a condensed, inactive X chromosome found in the nuclei of female cells

A

Barr bodies

24
Q

a genetic condition that arises due to an abnormality in the number or structure of chromosomes within a cell

A

Chromosomal disorders

25
causes genes to have abnormal numbers of chromosomes
Nondisjunction
26
Down Syndrome (trisonomy 21)
3 chromosomes at number 21
27
Turners syndrome
only one x chromosome
28
Klinefelter's syndrome
Extra x chromosome