Results 1 - 10 of 10,096 for 3S -"3-Hydroxyadipyl-CoA"
  1. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (also known as HMG-CoA lyase deficiency) is an uncommon inherited disorder in which the body cannot process ...
  2. 3-methylglutaconyl-CoA hydratase deficiency is an inherited condition that causes neurological problems. Beginning in infancy to early childhood, children ...
  3. Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is a rare condition that prevents the body from converting certain fats to energy, particularly ...
  4. Omega-3 fatty acids are a type of polyunsaturated fat . We need these fats to build brain cells and for other important functions. Omega-3s help keep your heart healthy and protected against ...
  5. 3-beta (β)-hydroxysteroid dehydrogenase (HSD) deficiency is an inherited disorder that affects hormone-producing glands including the gonads (ovaries in females ...
  6. Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is an inherited disorder that impairs the body's ability to break down ... instructions for making an enzyme called succinyl-CoA:3-ketoacid CoA transferase (SCOT). The SCOT enzyme is ...
  7. 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome, is a disorder caused by the loss ... of the chromosome at a location designated q13.3.The features of 22q13.3 deletion syndrome vary ...
  8. ... skills and growth markers that are relevant to 3-year-olds. ... provider. Physical and motor milestones for a typical 3-year-old include: Gains about 4 to 5 ...
  9. 15q13.3 microdeletion is a chromosomal change in which a small piece of chromosome 15 is deleted in each ... of the chromosome at a position designated q13.3. This chromosomal change increases the risk of intellectual ...
  10. 9q22.3 microdeletion is a chromosomal change in which a small piece of chromosome 9 is deleted in each ... of the chromosome in a region designated q22.3. This chromosomal change is associated with delayed development, ...
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