Glutaric Aciduria Type I<\/td> | <\/a><\/a><\/a><\/td> | Not Available<\/span><\/td><\/tr>Hyperlysinemia I, Familial<\/td> | <\/a><\/a><\/a><\/td> | Not Available<\/span><\/td><\/tr>Hyperlysinemia II or Saccharopinuria<\/td> | <\/a><\/a><\/a><\/td> | Not Available<\/span><\/td><\/tr>Long chain acyl-CoA dehydrogenase deficiency (LCAD)<\/td> | <\/a><\/a><\/a><\/td> | Not Available<\/span><\/td><\/tr><\/tbody><\/table> | | | |