inherited disorder in English

noun

genetic disorder, genetic disease, disorder that is transmitted genetically; pathological condition resulting from the absent or deficient gene, pathological condition caused by a chromosomal abnormality

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Below are sample sentences containing the word "inherited disorder" from the English Dictionary. We can refer to these sentence patterns for sentences in case of finding sample sentences with the word "inherited disorder", or refer to the context using the word "inherited disorder" in the English Dictionary.

1. Wilson’s Disease is a rare inherited disorder in which copper accumulates in tissues.

2. Wilson disease is an inherited disorder of copper transport, resulting in accumulation of copper in liver and brain.

3. Cystinosis is a recessively inherited disorder of amino acid metabolism resulting in the abnormal intracellular accumulation of cystine.

4. HoloCarboxylase synthetase deficiency is an inherited disorder in which the body is unable to use the vitamin biotin effectively

5. Agammaglobulinemia is an inherited disorder in which a person has very low levels of protective immune system proteins called immunoglobulins

6. Pyruvate Carboxylase deficiency is an inherited disorder that causes lactic acid and other potentially toxic compounds to accumulate in the blood

7. Autoimmune lymphoproliferative syndrome (Alps) is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes)

8. 3-methylcrotonyl-CoA Carboxylase deficiency (also known as 3-MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins properly

9. 3-methylcrotonyl-CoA Carboxylase deficiency (also known as 3-MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins properly.

10. 3-methylcrotonyl-CoA Carboxylase deficiency (also known as 3-MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins properly

11. Primary Ciliary dyskinesia (PCD) is an inherited disorder of clinical and genetic heterogeneity resulting from mutations in genes involved in the transport, assembly and function of motile cilia

12. Unlike Acquired cystic kidney disease, PKD is a genetic, or inherited, disorder that can cause complications such as high blood pressure and problems with blood vessels in the brain and heart.

13. Bartter syndrome is a rare inherited disorder that impedes the kidneys' ability to reabsorb salt, potassium, calcium, and other electrolytes, leading to the excessive loss of all of these compounds in urine.

14. Carbonic anhydrase VA deficiency is an inherited disorder characterized by episodes during which the balance of certain substances in the body is disrupted (known as metabolic crisis) and brain function is abnormal (known as acute encephalopathy)

15. Also known as Bruton's Agammaglobulinemia or congenital Agammaglobulinemia, X-Linked Agammaglobulinemia is an inherited disorder, occurring mainly in boys, in which your child is unable to produce antibodies (the body's primary defense against bacteria and viruses)

16. Asphyxiating thoracic dystrophy, also known as Jeune syndrome, is an inherited disorder of bone growth characterized by a narrow chest, short ribs, shortened bones in the arms and legs, short stature, and extra fingers and toes (polydactyly)

17. From GHRAsphyxiating thoracic dystrophy, also known as Jeune syndrome, is an inherited disorder of bone growth characterized by a narrow chest, short ribs, shortened bones in the arms and legs, short stature, and extra fingers and toes (polydactyly).

18. Pyruvate Carboxylase deficiency is an inherited disorder that causes lactic acid and other potentially toxic compounds to accumulate in the blood. High levels of these substances can damage the body's organs and tissues, particularly in the nervous system.

19. Primary Ciliary dyskinesia (PCD) is an inherited disorder which affects the movement of tiny hair-like structures on body cells, known as cilia. Cilia are present on many types of cells, and particularly on those in the respiratory tract

20. Primary Ciliary dyskinesia (PCD) is a rare inherited disorder caused by defects in the structure and/or function of cilia. Cilia are tiny hair-like structures, which are required to move fluids and particles in various parts of the body, including the airways.