Which one of the following is a hereditary disease? (1) Haemophilia (2) Myopia (3) Anaemia (4) Leukemia

Which one of the following is a hereditary disease? (1) Haemophilia (2) Myopia (3) Anaemia (4) Leukemia
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(1) Haemophilia Explanation: Hemophilia is a group of hereditary genetic disorders that impair the body's ability to control blood clotting or coagulation, which is used to stop bleeding when a blood vessel is broken. It has been associated with royal families due to inbreeding, and is sometimes called the 'Royal Disease.'
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Which one of the following is a hereditary disease ? (1) Haemophilia (2) Myopia (3) Anaemia (4) Leukemia

Description : Which one of the following is a hereditary disease ? (1) Haemophilia (2) Myopia (3) Anaemia (4) Leukemia

Last Answer : Haemophilia

Consider the following human diseases: 1. Anaemia 2. Haemophilia 3. Leukemia 4. Phenylketonuria Which of the above diseases are hereditary in nature? (a) 1, 2 and 3 (b) 1 and 4 (c) 2 and 3 (d) 2 and 4

Description : Consider the following human diseases: 1. Anaemia 2. Haemophilia 3. Leukemia 4. Phenylketonuria Which of the above diseases are hereditary in nature? (a) 1, 2 and 3 (b) 1 and 4 (c) 2 and 3 (d) 2 and 4

Last Answer : Ans:(d)

Haemophilia is a kind of disease which is (1) viral (2) bacterial (3) hereditary (4) fungal

Description : Haemophilia is a kind of disease which is (1) viral (2) bacterial (3) hereditary (4) fungal

Last Answer : (3) hereditary Explanation: Hemophilia A and hemophilia B are inherited in an X-linked recessive pattern. The genes associated with these conditions are located on the X chromosome, which is one of the two sex chromosomes.

Which one of the following is a hereditary disease? (1) Cataract (2) Haemophilia (3) Pellagra (4) Osteoporosis

Description : Which one of the following is a hereditary disease? (1) Cataract (2) Haemophilia (3) Pellagra (4) Osteoporosis

Last Answer : (2) Haemophilia Explanation: In this instance, a specific gene from one or both parents leads to an abnormality. Examples of such a condition would be sickle cell anemia, cystic fibrosis, or hemophilia.

Which one of the following is a hereditary disease? (1) Cataract (2) Haemophilia (3) Pellagra (4) Osteoporosis

Description : Which one of the following is a hereditary disease? (1) Cataract (2) Haemophilia (3) Pellagra (4) Osteoporosis

Last Answer : (2) Haemophilia Explanation: Haemophilia is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.

.Which of the following is not a hereditary disease? (a) Cystic fibrosis (b) Thalassaemia (c) Haemophilia (d) Cretinism

Description : .Which of the following is not a hereditary disease? (a) Cystic fibrosis (b) Thalassaemia (c) Haemophilia (d) Cretinism

Last Answer : (d) Cretinism

Which of the following is a correct match? (a) Down’s syndrome - 21st chromosome (b) Sickle cell anaemia - X-chromosome (c) Haemophilia - Y-chromosome (d) Parkinson’s disease - X and Y chromosome

Description : Which of the following is a correct match? (a) Down’s syndrome - 21st chromosome (b) Sickle cell anaemia - X-chromosome (c) Haemophilia - Y-chromosome (d) Parkinson’s disease - X and Y chromosome

Last Answer : a) Down’s syndrome - 21st chromosome

Pick out the correct statements. (1) Haemophilia is a sex-linked recessive disease. (2) Down’s syndrome is due to aneuploidy. (3) Phenylketonuria is an autosomal recessive gene disorder. (4) Sickle cell anaemia is an X-linked recessive gene disorder. (a) (1), (3) and (4) are correct. (b) (1), (2) and (3) are correct. (c) (1) and (4) are correct. (d) (2) and (4) are correct.

Description : Pick out the correct statements. (1) Haemophilia is a sex-linked recessive disease. (2) Down's syndrome is due to aneuploidy. (3) Phenylketonuria is an autosomal recessive gene disorder. (4) Sickle cell anaemia is an X- ... are correct. (c) (1) and (4) are correct. (d) (2) and (4) are correct.

Last Answer : (b) (1), (2) and (3) are correct.

Which one of the following statements is correct regarding sexually transmitted diseases (STDs)? (a) A person may contract syphilis by sharing milk with one already suffering from the disease. (b) Haemophilia is one of the STDs.(c) Genital herpes and sickle-cell anaemia are both STDs. (d) The chances of a 5-years boy contracting a STD are very little.

Description : Which one of the following statements is correct regarding sexually transmitted diseases (STDs)? (a) A person may contract syphilis by sharing milk with one already suffering from the disease. (b) Haemophilia is ... both STDs. (d) The chances of a 5-years boy contracting a STD are very little.

Last Answer : (d) The chances of a 5-years boy contracting a STD are very little.

Blood cancer is commonly known as – (1) Leucoderma (2) Leukaemia (3) Haemophilia (4) Sickle-cell. anaemia

Description : Blood cancer is commonly known as – (1) Leucoderma (2) Leukaemia (3) Haemophilia (4) Sickle-cell. anaemia

Last Answer : (2) Leukaemia Explanation: Leukemia is a cancer of blood and bone marrow. When a person has leukemia, the body makes too many white blood cells (leukocytes). The causes of most types of leukemia are not known. In general, all cancers have a breakdown in the normal way cell division is controlled.

Which one of the following is a condition of delayed blood clotting? (1) Heaemorrhage (2) Hematuria (3) Haemophilia (4) Anaemia

Description : Which one of the following is a condition of delayed blood clotting? (1) Heaemorrhage (2) Hematuria (3) Haemophilia (4) Anaemia

Last Answer : (3) Haemophilia Explanation: Haemophilia is a group of hereditary genetic disorders that impair the body's ability to control blood clotting or coagulation, which is used to stop bleeding when a blood vessel is broken.

.Represented here is the inheritance pattern of a certain type of trait in humans. Which one of the following conditions could be an example of this pattern? (a) Phenylketonuria (b) Sickle cell anaemia (c) Haemophilia (d) Thalassemia

Description : .Represented here is the inheritance pattern of a certain type of trait in humans. Which one of the following conditions could be an example of this pattern? (a) Phenylketonuria (b) Sickle cell anaemia (c) Haemophilia (d) Thalassemia

Last Answer : (c) Haemophilia

Select the correct match. (a) Haemophilia – Y linked (b) Phenylketonuria – Autosomal dominant trait(c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11 (d) Thalassemia – X linked

Description : Select the correct match. (a) Haemophilia – Y linked (b) Phenylketonuria – Autosomal dominant trait (c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11 (d) Thalassemia – X linked

Last Answer : (c) Sickle cell anaemia – Autosomal recessive trait,chromosome -11

Which of the following is an example of pleiotropy? (a) Haemophilia (b) Thalassemia (c) Sickle cell anaemia (d) Colour blindness

Description : Which of the following is an example of pleiotropy? (a) Haemophilia (b) Thalassemia (c) Sickle cell anaemia (d) Colour blindness

Last Answer : (c) Sickle cell anaemia

Which one of the following is a condition of delayed blood clotting? (1) Heaemorrhage (2) Hematuria (3) Haemophilia (4) Anaemia

Description : Which one of the following is a condition of delayed blood clotting? (1) Heaemorrhage (2) Hematuria (3) Haemophilia (4) Anaemia

Last Answer : Haemophilia

Myopia is a disease connected with – (1) Lungs (2) Brain (3) Ears (4) Eyes

Description : Myopia is a disease connected with – (1) Lungs (2) Brain (3) Ears (4) Eyes

Last Answer : (4) Eyes Explanation: Myopia, commonly known as nearsightedness, is a vision condition in which close objects are seen clearly, but objects' farther away appear blurred. It occurs if the eyeball ... eye has too much curvature. Concave lenses or corrective surgery is used to correct this defect.

A man cannot see clearly beyond 10 meters. The disease he suffers from : (1) Far sight (2) Myopia (3) Cataract (4) Hypermetropia

Description : A man cannot see clearly beyond 10 meters. The disease he suffers from : (1) Far sight (2) Myopia (3) Cataract (4) Hypermetropia

Last Answer : (2) Myopia Explanation: The man suffers from myopia, a vision condition in which close objects are seen clearly, but objects farther away appear blurred. Nearsightedness occurs if the eyeball is too ... a result, the light entering the eye isn't focused correctly and distant objects look blurred.

Myopia is a disease connected with-----? A. Ears B. Eyes (Answer) C. Lungs D. Brain

Description : Myopia is a disease connected with-----? A. Ears B. Eyes (Answer) C. Lungs D. Brain

Last Answer : B. Eyes (Answer)

Myopia is a disease connected with A.Ears B.Eyes C.Lungs D.Brain

Description : Myopia is a disease connected with A.Ears B.Eyes C.Lungs D.Brain

Last Answer : B.Eyes

Myopia is a disease connected with (1) Lungs (2) Brain (3) Ears (4) Eyes

Description : Myopia is a disease connected with (1) Lungs (2) Brain (3) Ears (4) Eyes

Last Answer : Eyes

A man cannot see clearly beyond 10 meters. The disease he suffers from : (1) Far sight (2) Myopia (3) Cataract (4) Hypermetropia

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$ Haemophilia is a sex linked disease ! Haemophilia is due to a recessive gene.

Description : $ Haemophilia is a sex linked disease ! Haemophilia is due to a recessive gene.

Last Answer : $ Haemophilia is a sex linked disease ! Haemophilia is due to a recessive gene. A. If both As and R are ... R is wrong D. If both As and R are wrong.

Abnormalities of blood clotting are (A) Haemophilia (B) ********* disease (C) Gout (D) Both (A) and (B)

Description : Abnormalities of blood clotting are (A) Haemophilia (B) Christmas disease (C) Gout (D) Both (A) and (B)

Last Answer : Answer : D

Haemophilia is a genetic disorder which leads to - (1) decrease in haemoglobin level (2) rheumatic heart disease (3) decrease in WBOC (4) non-clotting of blood

Description : Haemophilia is a genetic disorder which leads to - (1) decrease in haemoglobin level (2) rheumatic heart disease (3) decrease in WBOC (4) non-clotting of blood

Last Answer : (4) non-clotting of blood Explanation: Haemophilia is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.

Haemophilia is a genetic disorder which lead to – (1) decrease in haemoglobin level (2) rheumatic heart disease (3) decrease in WBC (4) non-clotting of blood

Description : Haemophilia is a genetic disorder which lead to – (1) decrease in haemoglobin level (2) rheumatic heart disease (3) decrease in WBC (4) non-clotting of blood

Last Answer : (4) non-clotting of blood Explanation: Haemophilia is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.

.********* disease is another name for (a) haemophilia B (b) hepatitis B (c) Down’s syndrome (d) sleeping sickness.

Description : .Christmas disease is another name for (a) haemophilia B (b) hepatitis B (c) Down’s syndrome (d) sleeping sickness.

Last Answer : a) haemophilia B

Haemophilia is more commonly seen in human males than in human females because (a) a greater proportion of girls die in infancy (b) this disease is due to a Y-linked recessive mutation (c) this disease is due to an X-linked recessive mutation (d) this disease is due to an X-linked dominant mutation.

Description : Haemophilia is more commonly seen in human males than in human females because (a) a greater proportion of girls die in infancy (b) this disease is due to a Y-linked recessive mutation (c) this ... to an X-linked recessive mutation (d) this disease is due to an X-linked dominant mutation.

Last Answer : this disease is due to an X-linked recessive mutation

Study the pedigree chart given below. What does it show? (a) Inheritance of a condition like phenylketonuria as an autosomal recessive trait. (b) The pedigree chart is wrong as this is not possible. (c) Inheritance of a recessive sex-linked disease like haemophilia. (d) Inheritance of a sex-linked inborn error of metabolism like phenylketonuria

Description : Study the pedigree chart given below. What does it show? (a) Inheritance of a condition like phenylketonuria as an autosomal recessive trait. (b) The pedigree chart is wrong as this is ... disease like haemophilia. (d) Inheritance of a sex-linked inborn error of metabolism like phenylketonuria

Last Answer : (a) Inheritance of a condition like phenylketonuria as an autosomal recessive trait.

Select the incorrect statement with regard to haemophilia. (a) It is a dominant disease.(b) A single protein involved in the clotting of blood is affected. (c) It is a sex-linked disease. (d) It is a recessive disease.

Description : Select the incorrect statement with regard to haemophilia. (a) It is a dominant disease. (b) A single protein involved in the clotting of blood is affected. (c) It is a sex-linked disease. (d) It is a recessive disease.

Last Answer : (a) It is a dominant disease.

Leukemia is a disease of the------? A. Lungs B. Blood (Answer) C. Skin D. Nerves

Description : Leukemia is a disease of the------? A. Lungs B. Blood (Answer) C. Skin D. Nerves

Last Answer : B. Blood (Answer)

Leukemia is a disease of the A.Lungs B.Blood C.Skin D.Nerves

Description : Leukemia is a disease of the A.Lungs B.Blood C.Skin D.Nerves

Last Answer : B.Blood

If cardiovascular disease is hereditary, what can I do to lower my risk?

Description : If cardiovascular disease is hereditary, what can I do to lower my risk?

Last Answer : If a disease is hereditary, there aren't many ways to prevent it except for asking your doctor for health advice and tips on how to change your lifestyle choices for yourself and those who you're worried about.

Is Alzheimer's disease hereditary?

Description : Is Alzheimer's disease hereditary?

Last Answer : Familial Alzheimer's disease (FAD) or early-onset Alzheimer's is an inherited, rare form of the disease, affecting less than 10 percent of Alzheimer's disease patients. FAD develops before age 65, in ... , clusters of cases are seen. Although a specific gene has not been identified as the cause o

Pentosuria is a rare hereditary disease is characterized by increased urinary excretion of (A) L-xylulose (B) Xylitol (C) Xylulose 5-phosphate (D) Ribose 5-phosphate

Description : Pentosuria is a rare hereditary disease is characterized by increased urinary excretion of (A) L-xylulose (B) Xylitol (C) Xylulose 5-phosphate (D) Ribose 5-phosphate

Last Answer : Answer : A

Thalassemia is a hereditary disease. It affects - (1) Blood (2) Spleen (3) Lungs (4) Heart

Description : Thalassemia is a hereditary disease. It affects - (1) Blood (2) Spleen (3) Lungs (4) Heart

Last Answer : (1) Blood Explanation: Thalassemia are forms of inherited autosomal recessive blood disorders that originated in the Mediterranean region. In thalassemia, the disease is caused by the weakening and destruction ... against malaria, which is or was prevalent in the regions where the trait is common.

Which one is a hereditary disease? (a) Cataract (b) Leprosy (c) Blindness (d) Phenylketonuria

Description : Which one is a hereditary disease? (a) Cataract (b) Leprosy (c) Blindness (d) Phenylketonuria

Last Answer : (d) Phenylketonuria

Degenerative neurologic disorders include which of the following? a) Huntington’s disease Huntington’s disease is a chronic, progressive, degenerative neurologic hereditary disease of the nervous system that results in progressive involuntary choreiform movement and dementia.

Description : Degenerative neurologic disorders include which of the following? a) Huntington's disease Huntington's disease is a chronic, progressive, degenerative neurologic hereditary disease of the nervous system that results in ... the bone. d) Glioma Malignant glioma is the most common type of brain tumor.

Last Answer : a) Huntington’s disease Huntington’s disease is a chronic, progressive, degenerative neurologic hereditary disease of the nervous system that results in progressive involuntary choreiform movement and dementia.

Which of the following diseases is a chronic, progressive, hereditary disease of the nervous system that results in progressive involuntary dance-like movement and dementia? a) Huntington’s disease Because it is transmitted as an autosomal dominant genetic disorder, each child of a parent with HD has a 50% risk of inheriting the illness.

Description : Which of the following diseases is a chronic, progressive, hereditary disease of the nervous system that results in progressive involuntary dance-like movement and dementia? a) Huntington's ... the central nervous system characterized by spongiform degeneration of the gray matter of the brain.

Last Answer : a) Huntington’s disease Because it is transmitted as an autosomal dominant genetic disorder, each child of a parent with HD has a 50% risk of inheriting the illness.

Rickets and kwashiorkor are (a) Deficiency disease (b) Hereditary disease (c) Infectious disease (d) Communicable disease

Description : Rickets and kwashiorkor are (a) Deficiency disease (b) Hereditary disease (c) Infectious disease (d) Communicable disease

Last Answer : (a) Deficiency disease

Thalassemia is a hereditary disease. It affects (1) Blood (2) Spleen (3) Lungs (4) Heart

Description : Thalassemia is a hereditary disease. It affects (1) Blood (2) Spleen (3) Lungs (4) Heart

Last Answer : Blood

Anaemia disease is caused by `:`

Description : Anaemia disease is caused by `:`

Last Answer : Anaemia disease is caused by `:` A. Deficiency of Fe B. Deficiency of Na C. Deficiency of Ca D. Deficiency of Mg

BMR is increased in all of the following except (A) Hyperthyroidism (B) Anaemia (C) Addison’s disease (D) Pregnancy

Description : BMR is increased in all of the following except (A) Hyperthyroidism (B) Anaemia (C) Addison’s disease (D) Pregnancy

Last Answer : Answer : C

Which vitamin deficiency causes the disease, Pernicious anaemia? (1) Vitamin B5 (2) Vitamin B12 (3) Vitamin B6 (4) Vitamin C

Description : Which vitamin deficiency causes the disease, Pernicious anaemia? (1) Vitamin B5 (2) Vitamin B12 (3) Vitamin B6 (4) Vitamin C

Last Answer : (2) Vitamin B12 Explanation: Pernicious anemia is one of many types of the larger family of megaloblastic anemias. It is caused by loss of gastric parietal cells which are responsible, in ... secretion of intrinsic factor, a protein essential for subsequent absorption of vitamin B12 in the ileum.

Which of the following is a skin disease? (1) Rickets (2) Osteomalacia (3) Anaemia (4) Pellagra

Description : Which of the following is a skin disease? (1) Rickets (2) Osteomalacia (3) Anaemia (4) Pellagra

Last Answer : (4) Pellagra Explanation: Pellagra is a disease caused by low levels of niacin, also known as vitamin B-3. It's marked by dementia, diarrhea, and dermatitis, also known as “the three Ds”.

Haemoglobin SC disease: a. is common amongst Afro-carribean people b. does not show sickle cells in the blood film. c. causes severe anaemia d. causes retinal vein occlusion

Description : Haemoglobin SC disease: a. is common amongst Afro-carribean people b. does not show sickle cells in the blood film. c. causes severe anaemia d. causes retinal vein occlusion

Last Answer : causes retinal vein occlusion

The following conditions give rise to red blood cells with increased mean cell volume: a. anaemia of chronic disease. b. pernicious anaemia. c. anaemia due to renal failure. d. haemolytic anaemi

Description : The following conditions give rise to red blood cells with increased mean cell volume: a. anaemia of chronic disease. b. pernicious anaemia. c. anaemia due to renal failure. d. haemolytic anaemi

Last Answer : pernicious anaemia.

.Which one of the following conditions though harmful in itself, is also potential saviour from a mosquito borne infectious disease ? (a) Thalassaemia (b) Sickle cell anaemia (c) Pernicious anaemia (d) Leukaemia

Description : .Which one of the following conditions though harmful in itself, is also potential saviour from a mosquito borne infectious disease ? (a) Thalassaemia (b) Sickle cell anaemia (c) Pernicious anaemia (d) Leukaemia

Last Answer : (b) Sickle cell anaemia

Sickle cell anaemia has not been eliminated from the African population because (a) it is controlled by dominant genes (b) it is controlled by recessive genes (c) it is not a fatal disease (d) it provides immunity against malaria

Description : Sickle cell anaemia has not been eliminated from the African population because (a) it is controlled by dominant genes (b) it is controlled by recessive genes (c) it is not a fatal disease (d) it provides immunity against malaria

Last Answer : (d) it provides immunity against malaria.

.A disease caused by an autosomal primary non- disjunction is (a) Klinefelter’s syndrome (b) Turner’s syndrome (c) Sickle cell anaemia (d) Down’s syndrome.

Description : .A disease caused by an autosomal primary non- disjunction is (a) Klinefelter’s syndrome (b) Turner’s syndrome (c) Sickle cell anaemia (d) Down’s syndrome.

Last Answer : (d) Down’s syndrome.

The most striking example of point mutation is found in a disease called (a) Down’s syndrome (b) sickle cell anaemia (c) thalassaemia (d) night blindness.

Description : The most striking example of point mutation is found in a disease called (a) Down’s syndrome (b) sickle cell anaemia (c) thalassaemia (d) night blindness.

Last Answer : (b) sickle cell anaemia