10: Genetic Vocabulary Flashcards

1
Q

Result from complex interaction of multiple genes in various sites.
May also be caused by interaction of genes with the environment.

A

Multifactorial (complex) gene disorders

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2
Q

Children receive two copies of one chromosome from one parent and none from the other parent.

A

Uniparental disomy

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3
Q

Abnormal development of an organ or large body part from an intrinsically abnormal process.

A

Malformation

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4
Q

Disorder that doesn’t fall into typical inheritance patterns.

A

Nontraditional inheritance disorder

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5
Q

Abnormal shape or position of body part caused by external mechanical forces.

A

Deformation

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6
Q

Probability a gene will be expressed.

A

Penetrance

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7
Q

Occurs only when a person has homozygous alleles.

A

Autosomal recessive

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8
Q

Less common because often fetus does not make it to term. Males frequently have worsened manifestation of disease.

A

X-linked dominant

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9
Q

Female carriers pass to their sons. Females may be carriers (heterozygous) or have condition (homozygous).

A

X-linked recessive

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10
Q

Typically cause neurodegenerative disorders.

Worsen with each generation.

A

Trinucleotide repeat disorders

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11
Q

Internally coded inheritable information.

A

Genotype

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12
Q

Abnormal organization of cells into tissues.

A

Dysplasia

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13
Q

A single gene is altered.

A

Single gene disorder

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14
Q

Mutation occurs in a cell of the developing organism after fertilization.

A

Germline mosaicism

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15
Q

Identifies missing, additional or rearranged chromosomal material.

A

FISH (Fluorescence in situ hybridization)

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16
Q

More likely to cluster in families.

A

Multifactorial (complex) gene disorders

17
Q

This DNA comes from ovum.

A

Mitochondrial DNA

18
Q

Multiple genes lead to problem.

A

Multifactorial disorder

19
Q

Can never be passed from father to son.

A

X-linked inheritance

20
Q

One gene dominates its counterpart from the other parent.

A

Autosomal dominant

21
Q

Defect of organ or large body part caused by external interruption of normal process.

A

Disruption

22
Q

Entire chromosome or large segment of it is missing or duplicated.

A

Chromosomal disorder

23
Q

Failure of pairs to separate properly during meiosis.

A

Nondisjunction anomalies

24
Q

The severity of disease may vary from person to person despite similar genotypes.

A

Variable expressivity

25
Q

For a female to have the condition, her father must be affected.

A

X-linked recessive

26
Q

Outward physical manifestation.

A

Phenotype

27
Q

Substances that can damage an embryo; NOT a genetic disorder.

A

Teratogens