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Studies have shown that antioxidant supplementation can alleviate muscle damage and protein oxidation induced by exercise

Direct chronotropic and inotropic effects of mildronate using cross-circulated dog atrial and ventricular preparations

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however, the pregnancy rate did not change significantly [19]

ENDOCRINE, NUTRITIONAL AND METABOLIC DISEASES E66.0 Obesity due to excess calories E66.01 Morbid (severe) obesity due to excess calories 5th Excludes1: morbid (severe) obesity with alveolar hypoventilation (E66.2) E66.09 Other obesity due to excess calories E66.1 Drug-induced obesity Use additional code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5) E66.2 Morbid (severe) obesity with alveolar hypoventilation obesity hypoventilation syndrome (OHS) Use with Z68.30 Z68.45 (adults) or Z68.53 (pediatrics, 2 20 yrs) Pickwickian syndrome E66.3 Overweight Use with Z68.25 Z68.29 (adults) or Z68.53 (pediatrics, 2 20 yrs) E66.8 Other obesity Use with Z68.30 Z68.45 (adults) or Z68.53 (pediatrics, 2 20 yrs) E66.9 Obesity, unspecified Use with Z68.30 Z68.45 (adults) or Z68.53 (pediatrics, 2 20 yrs) Obesity NOS E71.314 Muscle carnitine palmitoyltransferase deficiency E71.318 Other disorders of fatty-acid oxidation E71.32 Disorders of ketone metabolism E71.39 Other disorders of fatty-acid metabolism E71.4 Disorders of carnitine metabolism Excludes1: Muscle carnitine palmitoyltransferase deficiency 5th (E71.314) E71.40 Disorder of carnitine metabolism, unspecified E71.41 Primary carnitine deficiency E71.42 Carnitine deficiency due to inborn errors of metabolism Code also associated inborn error or metabolism E71.43 Iatrogenic carnitine deficiency Carnitine deficiency due to hemodialysis Carnitine deficiency due to Valproic acid therapy E71.44 Other secondary carnitine deficiency E71.440 Ruvalcaba-Myhre-Smith syndrome 6th E71.448 Other secondary carnitine deficiency E71.5 Peroxisomal disorders Excludes1: Schilders disease (G37.0) 5th E71.50 Peroxisomal disorder, unspecified E71.51 Disorders of peroxisome biogenesis Group 1 peroxisomal disorders 6th Excludes1: Refsums disease (G60.1) E71.510 Zellweger syndrome E71.511 Neonatal adrenoleukodystrophy Excludes1: X-linked adrenoleukodystrophy (E71.42-) E71.518 Other disorders of peroxisome biogenesis E71.52 X-linked adrenoleukodystrophy E71.520 Childhood cerebral X-linked 6th adrenoleukodystrophy E71.521 Adolescent X-linked adrenoleukodystrophy E71.522 Adrenomyeloneuropathy E71.528 Other X-linked adrenoleukodystrophy Addison only phenotype adrenoleukodystrophy Addison-Schilder adrenoleukodystrophy E71.529 X-linked adrenoleukodystrophy, unspecified type E71.53 Other group 2 peroxisomal disorders E71.54 Other peroxisomal disorders E71.540 Rhizomelic chondrodysplasia punctata 6th Excludes1: chondrodysplasia punctata NOS (Q77.3) E71.541 Zellweger-like syndrome E71.542 Other group 3 peroxisomal disorders E71.548 Other peroxisomal disorders (E70 E88) METABOLIC DISORDERS Excludes1: androgen insensitivity syndrome (E34.5-) congenital adrenal hyperplasia (E25.0) Ehlers-Danlos syndrome (Q79.6) hemolytic anemias attributable to enzyme disorders (D55.-) Marfans syndrome (Q87.4) 5-alpha-reductase deficiency (E29.1) E70 DISORDERS OF AROMATIC AMINO-ACID METABOLISM 4th E70.0 Classical phenylketonuria E71 DISORDERS OF BRANCHED-CHAIN AMINO-ACID METABOLISM AND FATTY-ACID METABOLISM 4th E71.0 Maple-syrup-urine disease E71.1 Other disorders of branched-chain amino-acid metabolism E71.11 Branched-chain organic acidurias 5th E71.110 Isovaleric acidemia 6th E71.111 3-methylglutaconic aciduria E71.118 Other branched-chain organic acidurias E71.12 Disorders of propionate metabolism E71.120 Methylmalonic acidemia 6th E71.121 Propionic acidemia E71.128 Other disorders of propionate metabolism E71.19 Other disorders of branched-chain amino-acid metabolism Hyperleucine-isoleucinemia Hypervalinemia E71.2 Disorder of branched-chain amino-acid metabolism, unspecified E71.3 Disorders of fatty-acid metabolism Excludes1: peroxisomal disorders (E71.5) 5th Refsums disease (G60.1) Schilders disease (G37.0) Excludes2: carnitine deficiency due to inborn error of metabolism (E71.42) E71.30 Disorder of fatty-acid metabolism, unspecified E71.31 Disorders of fatty-acid oxidation E71.310 Long chain/very long chain acyl CoA 6th dehydrogenase deficiency LCAD VLCAD E71.311 Medium chain acyl CoA dehydrogenase deficiency MCAD E71.312 Short chain acyl CoA dehydrogenase deficiency SCAD E71.313 Glutaric aciduria type II Glutaric aciduria type II A Glutaric aciduria type II B Glutaric aciduria type II C Excludes1: glutaric aciduria (type 1) NOS (E72.3) 4th 5th 164 ICD_10-4th_ed.indb 164 6th 7th Additional Character Required 3-character code (E00 E89) E72 OTHER DISORDERS OF AMINO-ACID METABOLISM 4th Excludes1: disorders of aromatic amino-acid metabolism (E70.-) branched-chain amino-acid metabolism (E71.0 E71.2) fatty-acid metabolism (E71.3) purine and pyrimidine metabolism (E79.-) gout (M1A.-, M10.-) E72.0 Disorders of amino-acid transport Excludes1: disorders of tryptophan metabolism (E70.5) 5th E72.00 Disorders of amino-acid transport, unspecified E72.01 Cystinuria E72.02 Hartnups disease E72.03 Lowes syndrome Use additional code for associated glaucoma (H42) E72.04 Cystinosis E72.5 Disorders of glycine metabolism E72.50 Disorder of glycine metabolism, unspecified 5th E72.51 Non-ketotic hyperglycinemia E72.52 Trimethylaminuria E72.53 Primary hyperoxaluria Oxalosis Oxaluria =New Code =Revised Code Excludes1Not coded here, do not use together Excludes2Not included here PEDIATRIC ICD-10-CM 2019: A MANUAL FOR PROVIDER-BASED CODING 8/16/18 5:33 PM TABULAR LIST CHAPTER 4