Results 1 - 10 of 1,233 for S -"3-Hydroxyhexadecanoyl-CoA"
  1. Protein S deficiency is a disorder of blood clotting. People with this condition have an increased risk of developing abnormal blood clots.Individuals with mild protein S deficiency are at risk of a type of ...
  2. Thiopurine S-methyltransferase (TPMT) deficiency is a condition characterized by significantly reduced activity of an enzyme that helps the body process drugs called ...
  3. ... phenomenon is a condition in which the body's normal response to cold or emotional stress is ... the immune system malfunctions and attacks the body's own tissues and organs. Autoimmune disorders with which ...
  4. ... development. As a result, some of the body's cells have a normal version of the GNAS ... passed to the next generation. Albright syndrome Albright's disease Albright's disease of bone Albright's ...
  5. ... appears in adulthood, most often in a person's 40s or 50s. It is much less common ... that are related to sound and the body's position and movement.Researchers have studied many possible ...
  6. ... inherited disorder that affects many of the body's organs and tissues. The signs and symptoms of ... Cerebroside lipidosis syndrome Gaucher splenomegaly Gaucher syndrome Gaucher's disease Gauchers disease GD Glucocerebrosidase deficiency Glucocerebrosidosis Glucosyl ...
  7. ... of this disorder, usually appears in a person's thirties or forties. Early signs and symptoms can ... Huntington chorea Huntington chronic progressive hereditary chorea Huntington's chorea Huntington's disease Genetic Testing Registry: Huntington ...
  8. ... of the condition. Huntington disease-like syndromes Huntington's disease phenocopies Huntington's disease phenocopy syndromes Huntington's disease-like syndromes ...
  9. ... this disease have atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a ... abnormal version of beta-globin known as hemoglobin S (HbS). Other mutations in the HBB gene lead ...
  10. ... Although this condition usually begins in a person's teens or twenties, rare cases may appear in ... Leber hereditary optic atrophy Leber optic atrophy Leber's hereditary optic neuropathy Leber's optic atrophy Leber' ...
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