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E56.8 Deficiency of other vitamins |
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E56.9 Vitamin deficiency, unspecified |
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E58. Dietary calcium deficiency |
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E59. Dietary selenium deficiency |
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E60. Dietary zinc deficiency |
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E61.0 Copper deficiency |
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E61.1 Iron deficiency |
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E61.2 Magnesium deficiency |
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E61.3 Manganese deficiency |
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E61.4 Chromium deficiency |
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E61.5 Molybdenum deficiency |
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E61.6 Vanadium deficiency |
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E61.7 Deficiency of multiple nutrient elements |
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E61.8 Deficiency of other specified nutrient elements |
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E61.9 Deficiency of nutrient element, unspecified |
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E63.0 Essential fatty acid [EFA] deficiency |
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E63.1 Imbalance of constituents of food intake |
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E63.8 Other specified nutritional deficiencies |
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E63.9 Nutritional deficiency, unspecified |
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E64.0 Sequelae of protein-calorie malnutrition |
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E64.1 Sequelae of vitamin A deficiency |
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E64.2 Sequelae of vitamin C deficiency |
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E64.3 Sequelae of rickets |
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E64.8 Sequelae of other nutritional deficiencies |
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E64.9 Sequelae of unspecified nutritional deficiency |
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E65. Localized adiposity |
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E66.01 Morbid (severe) obesity due to excess calories |
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E66.09 Other obesity due to excess calories |
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E66.1 Drug-induced obesity |
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E66.2 Morbid (severe) obesity with alveolar hypoventilation |
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E66.3 Overweight |
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E66.8 Other obesity |
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E66.9 Obesity, unspecified |
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E67.0 Hypervitaminosis A |
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E67.1 Hypercarotenemia |
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E67.2 Megavitamin-B6 syndrome |
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E67.3 Hypervitaminosis D |
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E67.8 Other specified hyperalimentation |
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E68. Sequelae of hyperalimentation |
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E70.0 Classical phenylketonuria |
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E70.1 Other hyperphenylalaninemias |
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E70.20 Disorder of tyrosine metabolism, unspecified |
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E70.21 Tyrosinemia |
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E70.29 Other disorders of tyrosine metabolism |
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E70.30 Albinism, unspecified |
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E70.310 X-linked ocular albinism |
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E70.311 Autosomal recessive ocular albinism |
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E70.318 Other ocular albinism |
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E70.319 Ocular albinism, unspecified |
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E70.320 Tyrosinase negative oculocutaneous albinism |
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E70.321 Tyrosinase positive oculocutaneous albinism |
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E70.328 Other oculocutaneous albinism |
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E70.329 Oculocutaneous albinism, unspecified |
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E70.330 Chediak-Higashi syndrome |
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E70.331 Hermansky-Pudlak syndrome |
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E70.338 Other albinism with hematologic abnormality |
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E70.339 Albinism with hematologic abnormality, unspecified |
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E70.39 Other specified albinism |
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E70.40 Disorders of histidine metabolism, unspecified |
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E70.41 Histidinemia |
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E70.49 Other disorders of histidine metabolism |
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E70.5 Disorders of tryptophan metabolism |
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E70.81 Aromatic L-amino acid decarboxylase deficiency |
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E70.89 Other disorders of aromatic amino-acid metabolism |
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E70.9 Disorder of aromatic amino-acid metabolism, unspecified |
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E71.0 Maple-syrup-urine disease |
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E71.110 Isovaleric acidemia |
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E71.111 3-methylglutaconic aciduria |
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E71.118 Other branched-chain organic acidurias |
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E71.120 Methylmalonic acidemia |
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E71.121 Propionic acidemia |
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E71.128 Other disorders of propionate metabolism |
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E71.19 Other disorders of branched-chain amino-acid metabolism |
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E71.2 Disorder of branched-chain amino-acid metabolism, unspecified |
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E71.30 Disorder of fatty-acid metabolism, unspecified |
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E71.310 Long chain/very long chain acyl CoA dehydrogenase deficiency |
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E71.311 Medium chain acyl CoA dehydrogenase deficiency |
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E71.312 Short chain acyl CoA dehydrogenase deficiency |
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E71.313 Glutaric aciduria type II |
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E71.314 Muscle carnitine palmitoyltransferase deficiency |
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E71.318 Other disorders of fatty-acid oxidation |
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E71.32 Disorders of ketone metabolism |
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E71.39 Other disorders of fatty-acid metabolism |
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E71.40 Disorder of carnitine metabolism, unspecified |
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E71.41 Primary carnitine deficiency |
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E71.42 Carnitine deficiency due to inborn errors of metabolism |
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E71.43 Iatrogenic carnitine deficiency |
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E71.440 Ruvalcaba-Myhre-Smith syndrome |
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E71.448 Other secondary carnitine deficiency |
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E71.50 Peroxisomal disorder, unspecified |
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E71.510 Zellweger syndrome |
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E71.511 Neonatal adrenoleukodystrophy |
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E71.518 Other disorders of peroxisome biogenesis |
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E71.520 Childhood cerebral X-linked adrenoleukodystrophy |
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E71.521 Adolescent X-linked adrenoleukodystrophy |
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E71.522 Adrenomyeloneuropathy |
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E71.528 Other X-linked adrenoleukodystrophy |
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E71.529 X-linked adrenoleukodystrophy, unspecified type |
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E71.53 Other group 2 peroxisomal disorders |
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E71.540 Rhizomelic chondrodysplasia punctata |
