3.12: Genetic Disorders - Biology

Is being short-statured inherited?

It can be. Achondroplasia is the most common form of dwarfism in humans, and it is caused by a dominant mutation. The mutation can be passed from one generation to the next.

Genetic Disorders

Many genetic disorders are caused by mutations in one or a few genes. Other genetic disorders are caused by abnormal numbers of chromosomes.

Genetic Disorders Caused by Mutations

The Table below lists several genetic disorders caused by mutations in just one gene. Some of the disorders are caused by mutations in autosomal genes, others by mutations in X-linked genes. Which disorder would you expect to be more common in males than females? You can watch a video about the human genome, genetic disorders, and mutations at this link:

You can click on any human chromosome at this link to see the genetic disorders associated with it:

Genetic DisorderDirect Effect of MutationSigns and Symptoms of the DisorderMode of Inheritance
Marfan syndromedefective protein in connective tissueheart and bone defects and unusually long, slender limbs and fingersautosomal dominant
Sickle cell anemiaabnormal hemoglobin protein in red blood cellssickle-shaped red blood cells that clog tinyblood vessels, causing pain and damaging organs and jointsautosomal recessive
Vitamin D-resistant ricketslack of a substance needed for bones to absorb mineralssoft bones that easily become deformed, leading to bowed legs and other skeletal deformitiesX-linked dominant
Hemophilia Areduced activity of a protein needed for blood clottinginternal and external bleeding that occurs easily and is difficult to controlX-linked recessive

Few genetic disorders are controlled by dominant alleles. A mutant dominant allele is expressed in every individual who inherits even one copy of it. If it causes a serious disorder, affected people may die young and fail to reproduce. Therefore, the mutant dominant allele is likely to die out of the population.

A mutant recessive allele, such as the allele that causes sickle cell anemia (see Figure belowand the link that follows), is not expressed in people who inherit just one copy of it. These people are called carriers. They do not have the disorder themselves, but they carry the mutant allele and can pass it to their offspring. Thus, the allele is likely to pass on to the next generation rather than die out.

Sickle-Shaped and Normal Red Blood Cells. Sickle cell anemia is an autosomal recessive disorder. The mutation that causes the disorder affects just one amino acid in a single protein, but it has serious consequences for the affected person. This photo shows the sickle shape of red blood cells in people with sickle cell anemia.

Cystic Fibrosis and Tay-Sachs disease are two additional severe genetic disorders. They are discussed in the following video: (9:31). Tay-Sachs is further discussed at (3:13) and (2:01).

Chromosomal Disorders

Mistakes may occur during meiosis that result in nondisjunction. This is the failure of replicated chromosomes to separate during meiosis (the animation at the link below shows how this happens). Some of the resulting gametes will be missing a chromosome, while others will have an extra copy of the chromosome. If such gametes are fertilized and form zygotes, they usually do not survive. If they do survive, the individuals are likely to have serious genetic disorders. Table below lists several genetic disorders that are caused by abnormal numbers of chromosomes. Most chromosomal disorders involve the X chromosome. Look back at the X and Y chromosomes and you will see why. The X and Y chromosomes are very different in size, so nondisjunction of the sex chromosomes occurs relatively often.

Genetic DisorderGenotypePhenotypic Effects
Down syndromeextra copy (complete or partial) of chromosome 21 (see Figure below)developmental delays, distinctive facial appearance, and other abnormalities (see Figurebelow)
Turner’s syndromeone X chromosome but no other sex chromosome (XO)female with short height and infertility (inability to reproduce)
Triple X syndromethree X chromosomes (XXX)female with mild developmental delays and menstrual irregularities
Klinefelter’s syndromeone Y chromosome and two or more X chromosomes (XXY, XXXY)male with problems in sexual development and reduced levels of the male hormone testosterone

(left) Trisomy 21 (Down Syndrome) Karyotype. A karyotype is a picture of a cell's chromosomes. Note the extra chromosome 21. (right) Child with Down syndrome, exhibiting characteristic facial appearance.

Diagnosing Genetic Disorders

A genetic disorder that is caused by a mutation can be inherited. Therefore, people with a genetic disorder in their family may be concerned about having children with the disorder. Professionals known as genetic counselors can help them understand the risks of their children being affected. If they decide to have children, they may be advised to have prenatal(“before birth”) testing to see if the fetus has any genetic abnormalities. One method of prenatal testing is amniocentesis. In this procedure, a few fetal cells are extracted from the fluid surrounding the fetus, and the fetal chromosomes are examined.

Treating Genetic Disorders

The symptoms of genetic disorders can sometimes be treated, but cures for genetic disorders are still in the early stages of development. One potential cure that has already been used with some success is gene therapy. This involves inserting normal genes into cells with mutant genes. At the following link, you can watch the video ‘‘Sickle Cell Anemia: Hope fromGene Therapy’’, to learn how scientists are trying to cure sickle-cell anemia with gene therapy.

If you could learn your risk of getting cancer or another genetic disease, would you? Though this is a personal decision, it is a possibility. A number of companies now makes it easy to order medical genetic tests through the Web. See Genetic Testing through the Web at


  • Many genetic disorders are caused by mutations in one or a few genes.
  • Other genetic disorders are caused by abnormal numbers of chromosomes.

Explore More

Use this resource to answer the questions that follow.

  • Genetic Disorders at
  1. How do mutations affect proteins?
  2. What is a single-gene disorder?
  3. What is a chromosomal disorder?
  4. What is a complex disorder?
  5. Give an example of a chromosomal disorder.


  1. Describe a genetic disorder caused by a mutation in a single gene.
  2. What causes Down syndrome?
  3. What is nondisjunction?
  4. What is gene therapy?
  5. Explain why genetic disorders caused by abnormal numbers of chromosomes most often involve the X chromosome.


The following list includes the most common signs and symptoms in people with progeria. These features may be different from person to person. Some people may have more symptoms than others, and they can range from mild to severe. This list does not include every symptom that has been described in the condition.

  • Poor growth (failure to thrive)
  • Large head size relative to face
  • Loss of fat under the skin
  • Delayed eruption of teeth and other dental abnormalities
  • Baldness (alopecia)
  • Stiff joints
  • Thin, weak bones ( osteoporosis )
  • Progressive heart disease
  • Normal intelligence

This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.

Watch the video: Genommutationen: Trisomie, Monosomie, Geschlechts-Anomalien, Down-Syndrom - 3. Genetik (January 2022).