Mendelian Genetics
Basic Human Inheritance
Genetic Diseases
Mitosis
General Knowledge
100

Monk who began the study of genetics.

Mendel

100

Chart showing inheritance of a trait over several generations.

Pedigree

100

A disorder that affects the mucous-producing glands, digestive enzymes, and sweat glands.

Cystic fibrosis

100

The first and longest phase of mitosis.

Prophase

100

The process of cytoplasm division.

Cytokinesis

200

Observable characteristics of an allele pair.

Phenotype

200

An individual who is heterozygous for a recessive disorder.

Carrier

200

Gangliosides accumulate in the brain, inflating brain nerve cells and causing mental deterioration.  

Tay-Sachs disease

200

Mitotic phase where the chromatids pull apart. 

Anaphase

200

Structure where sister chromatids are attached.

Centromere

300

An organism with two of the same alleles for a trait.

Homozygous

300

True/False:

Pedigrees can be used to examine both recessive and dominant genetic disorders.

True

300

Genetic disorder characterized by the inability of the body to digest milk and milk products.

Galactosemia

300

The second and shortest mitotic phase. 

Metaphase

300

Spindle fibers, centrioles, and aster fibers form this.

Spindle apparatus

400

An organism with two different alleles for a particular trait.

Heterozygous

400

Daily Double

+2 on the next question.

400

Causes small body size and limbs that are comparatively short.  

Achondroplasia

400

Mitotic phase when the chromosomes arrive at the cell poles and begin to decondense.  

Telophase

400

Abbreviation for Parent Generation.

P generation

500

The allele that will be masked in a heterozygous pair.

Recessive gene

500

Affects the nervous system, causing gradual loss of brain function.

Huntington's disease

500

Individuals have very pale skin, white hair, and pink irises.  

Albinism

500

Structures that contain identical copies of DNA.

Chromatin

500

An organism's allele pairs. 

Genotype

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