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10
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9,600
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3S -"3-Hydroxyadipyl-CoA"
- 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 ...
- 3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins. ...
- 3-methylglutaconyl-CoA hydratase deficiency is an inherited condition that causes neurological problems. Beginning in infancy to early childhood, children ...
- 3-hydroxyacyl-CoA dehydrogenase deficiency is an inherited condition that prevents the body from converting certain fats to energy, particularly during ...
- Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is a rare condition that prevents the body from converting certain fats to energy, particularly ...
- 3-beta (β)-hydroxysteroid dehydrogenase (HSD) deficiency is an inherited disorder that affects hormone-producing glands including the gonads (ovaries in females ...
- 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 ...
- 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 ...
- 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 ...
- 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, ...