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Results 1 - 10 of 1,484 for Caused
  1. What are complex or multifactorial disorders?: MedlinePlus Genetics 
    ... as sickle cell disease and cystic fibrosis , are caused by variants (also known as mutations) in single ... such as exercise, diet, or pollutant exposures. Conditions caused by many contributing factors are called complex or ...
    https://medlineplus.gov/.../mutationsanddisorders/complexdisorders - Genetics
  2. Isolated growth hormone deficiency 
    Isolated growth hormone deficiency is a condition caused by a severe shortage or absence of growth hormone. Growth hormone is a protein that is necessary for the normal growth of the ...
    https://medlineplus.gov/.../isolated-growth-hormone-deficiency - Genetics
  3. What are the different ways a genetic condition can be inherited?: MedlinePlus Genetics 
    Some genetic conditions are caused by variants (also known as mutations) in a single gene. These conditions are usually inherited in one of several patterns, ...
    https://medlineplus.gov/.../inheritance/inheritancepatterns - Genetics
  4. Pseudohypoaldosteronism type 2 
    Pseudohypoaldosteronism type 2 (PHA2) is caused by problems that affect regulation of the amount of sodium and potassium in the body. Sodium and potassium are important in ... however, the prevalence is unknown. PHA2 can be caused by mutations in the WNK1, WNK4, CUL3, or ...
    https://medlineplus.gov/.../condition/pseudohypoaldosteronism-type-2 - Genetics
  5. Glycogen storage disease type IX 
    ... also known as GSD IX) is a condition caused by the inability to break down a complex ... on the genetic cause of the condition.When caused by mutations in the PHKA1 or PHKA2 gene, ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-ix - Genetics
  6. Tetrahydrobiopterin deficiency 
    ... of elevated phenylalanine levels. The remaining cases are caused by a similar condition called phenylketonuria (PKU). In ... common for elevated levels of phenylalanine to be caused by tetrahydrobiopterin deficiency than by PKU. Tetrahydrobiopterin deficiency ...
    https://medlineplus.gov/.../condition/tetrahydrobiopterin-deficiency - Genetics
  7. Hypomagnesemia with secondary hypocalcemia 
    Hypomagnesemia with secondary hypocalcemia is an inherited condition caused by the body's inability to absorb and ... prevalence is unknown. Hypomagnesemia with secondary hypocalcemia is caused by mutations in the TRPM6 gene. This gene ...
    https://medlineplus.gov/...ypomagnesemia-with-secondary-hypocalcemia - Genetics
  8. Hartnup disease 
    Hartnup disease is a condition caused by the body's inability to absorb certain protein building blocks (amino acids) from the diet. As a result, affected individuals ...
    https://medlineplus.gov/genetics/condition/hartnup-disease - Genetics
  9. Carpal tunnel syndrome 
    Carpal tunnel syndrome is a disorder caused by disturbances in nerve function (neuropathy), leading to pain and numbness or tingling (paresthesia) primarily in the wrist and hand. While carpal ...
    https://medlineplus.gov/genetics/condition/carpal-tunnel-syndrome - Genetics
  10. Cushing disease 
    Cushing disease is caused by elevated levels of a hormone called cortisol, which leads to a wide variety of signs and symptoms. This ... can develop a hump on their upper back caused by abnormal deposits of fat. People with this ...
    https://medlineplus.gov/genetics/condition/cushing-disease - Genetics
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