Online 2016 ICD-10-CM · Tabular List · Alpha Index · ICD-9/ICD-10 conversion · ICD-10-PCS

E70Disorders of aromatic amino-acid metabolism
E70.0Classical phenylketonuria
E70.1Other hyperphenylalaninemias
E70.2Disorders of tyrosine metabolism
E70.20Disorder of tyrosine metabolism, unspecified
E70.29Other disorders of tyrosine metabolism
E70.30Albinism, unspecified
E70.31Ocular albinism
E70.310X-linked ocular albinism
E70.311Autosomal recessive ocular albinism
E70.318Other ocular albinism
E70.319Ocular albinism, unspecified
E70.32Oculocutaneous albinism
E70.320Tyrosinase negative oculocutaneous albinism
E70.321Tyrosinase positive oculocutaneous albinism
E70.328Other oculocutaneous albinism
E70.329Oculocutaneous albinism, unspecified
E70.33Albinism with hematologic abnormality
E70.330Chediak-Higashi syndrome
E70.331Hermansky-Pudlak syndrome
E70.338Other albinism with hematologic abnormality
E70.339Albinism with hematologic abnormality, unspecified
E70.39Other specified albinism
E70.4Disorders of histidine metabolism
E70.40Disorders of histidine metabolism, unspecified
E70.49Other disorders of histidine metabolism
E70.5Disorders of tryptophan metabolism
E70.8Other disorders of aromatic amino-acid metabolism
E70.9Disorder of aromatic amino-acid metabolism, unspecified
E71Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
E71.0Maple-syrup-urine disease
E71.1Other disorders of branched-chain amino-acid metabolism
E71.11Branched-chain organic acidurias
E71.110Isovaleric acidemia
E71.1113-methylglutaconic aciduria
E71.118Other branched-chain organic acidurias
E71.12Disorders of propionate metabolism
E71.120Methylmalonic acidemia
E71.121Propionic acidemia
E71.128Other disorders of propionate metabolism
E71.19Other disorders of branched-chain amino-acid metabolism
E71.2Disorder of branched-chain amino-acid metabolism, unspecified
E71.3Disorders of fatty-acid metabolism
E71.30Disorder of fatty-acid metabolism, unspecified
E71.31Disorders of fatty-acid oxidation
E71.310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71.311Medium chain acyl CoA dehydrogenase deficiency
E71.312Short chain acyl CoA dehydrogenase deficiency
E71.313Glutaric aciduria type II
E71.314Muscle carnitine palmitoyltransferase deficiency
E71.318Other disorders of fatty-acid oxidation
E71.32Disorders of ketone metabolism
E71.39Other disorders of fatty-acid metabolism
E71.4Disorders of carnitine metabolism
E71.40Disorder of carnitine metabolism, unspecified
E71.41Primary carnitine deficiency
E71.42Carnitine deficiency due to inborn errors of metabolism
E71.43Iatrogenic carnitine deficiency
E71.44Other secondary carnitine deficiency
E71.440Ruvalcaba-Myhre-Smith syndrome
E71.448Other secondary carnitine deficiency
E71.5Peroxisomal disorders
E71.50Peroxisomal disorder, unspecified
E71.51Disorders of peroxisome biogenesis
E71.510Zellweger syndrome
E71.511Neonatal adrenoleukodystrophy
E71.518Other disorders of peroxisome biogenesis
E71.52X-linked adrenoleukodystrophy
E71.520Childhood cerebral X-linked adrenoleukodystrophy
E71.521Adolescent X-linked adrenoleukodystrophy
E71.528Other X-linked adrenoleukodystrophy
E71.529X-linked adrenoleukodystrophy, unspecified type
E71.53Other group 2 peroxisomal disorders
E71.54Other peroxisomal disorders
E71.540Rhizomelic chondrodysplasia punctata
E71.541Zellweger-like syndrome
E71.542Other group 3 peroxisomal disorders
E71.548Other peroxisomal disorders
E72Other disorders of amino-acid metabolism
E72.0Disorders of amino-acid transport
E72.00Disorders of amino-acid transport, unspecified
E72.02Hartnup's disease
E72.03Lowe's syndrome
E72.09Other disorders of amino-acid transport
E72.1Disorders of sulfur-bearing amino-acid metabolism
E72.10Disorders of sulfur-bearing amino-acid metabolism, unspecified
E72.12Methylenetetrahydrofolate reductase deficiency
E72.19Other disorders of sulfur-bearing amino-acid metabolism
E72.2Disorders of urea cycle metabolism
E72.20Disorder of urea cycle metabolism, unspecified
E72.22Arginosuccinic aciduria
E72.29Other disorders of urea cycle metabolism
E72.3Disorders of lysine and hydroxylysine metabolism
E72.4Disorders of ornithine metabolism
E72.5Disorders of glycine metabolism
E72.50Disorder of glycine metabolism, unspecified
E72.51Non-ketotic hyperglycinemia
E72.59Other disorders of glycine metabolism
E72.8Other specified disorders of amino-acid metabolism
E72.9Disorder of amino-acid metabolism, unspecified
E73Lactose intolerance
E73.0Congenital lactase deficiency
E73.1Secondary lactase deficiency
E73.8Other lactose intolerance
E73.9Lactose intolerance, unspecified
E74Other disorders of carbohydrate metabolism
E74.0Glycogen storage disease
E74.00Glycogen storage disease, unspecified
E74.01von Gierke disease
E74.02Pompe disease
E74.03Cori disease
E74.04McArdle disease
E74.09Other glycogen storage disease
E74.1Disorders of fructose metabolism
E74.10Disorder of fructose metabolism, unspecified
E74.11Essential fructosuria
E74.12Hereditary fructose intolerance
E74.19Other disorders of fructose metabolism
E74.2Disorders of galactose metabolism
E74.20Disorders of galactose metabolism, unspecified
E74.29Other disorders of galactose metabolism
E74.3Other disorders of intestinal carbohydrate absorption
E74.31Sucrase-isomaltase deficiency
E74.39Other disorders of intestinal carbohydrate absorption
E74.4Disorders of pyruvate metabolism and gluconeogenesis
E74.8Other specified disorders of carbohydrate metabolism
E74.9Disorder of carbohydrate metabolism, unspecified
E75Disorders of sphingolipid metabolism and other lipid storage disorders
E75.0GM2 gangliosidosis
E75.00GM2 gangliosidosis, unspecified
E75.01Sandhoff disease
E75.02Tay-Sachs disease
E75.09Other GM2 gangliosidosis
E75.1Other and unspecified gangliosidosis
E75.10Unspecified gangliosidosis
E75.11Mucolipidosis IV
E75.19Other gangliosidosis
E75.2Other sphingolipidosis
E75.21Fabry (-Anderson) disease
E75.22Gaucher disease
E75.23Krabbe disease
E75.24Niemann-Pick disease
E75.240Niemann-Pick disease type A
E75.241Niemann-Pick disease type B
E75.242Niemann-Pick disease type C
E75.243Niemann-Pick disease type D
E75.248Other Niemann-Pick disease
E75.249Niemann-Pick disease, unspecified
E75.25Metachromatic leukodystrophy
E75.29Other sphingolipidosis
E75.3Sphingolipidosis, unspecified
E75.4Neuronal ceroid lipofuscinosis
E75.5Other lipid storage disorders
E75.6Lipid storage disorder, unspecified
E76Disorders of glycosaminoglycan metabolism
E76.0Mucopolysaccharidosis, type I
E76.01Hurler's syndrome
E76.02Hurler-Scheie syndrome
E76.03Scheie's syndrome
E76.1Mucopolysaccharidosis, type II
E76.2Other mucopolysaccharidoses
E76.21Morquio mucopolysaccharidoses
E76.210Morquio A mucopolysaccharidoses
E76.211Morquio B mucopolysaccharidoses
E76.219Morquio mucopolysaccharidoses, unspecified
E76.22Sanfilippo mucopolysaccharidoses
E76.29Other mucopolysaccharidoses
E76.3Mucopolysaccharidosis, unspecified
E76.8Other disorders of glucosaminoglycan metabolism
E76.9Glucosaminoglycan metabolism disorder, unspecified
E77Disorders of glycoprotein metabolism
E77.0Defects in post-translational modification of lysosomal enzymes
E77.1Defects in glycoprotein degradation
E77.8Other disorders of glycoprotein metabolism
E77.9Disorder of glycoprotein metabolism, unspecified
E78Disorders of lipoprotein metabolism and other lipidemias
E78.0Pure hypercholesterolemia
E78.1Pure hyperglyceridemia
E78.2Mixed hyperlipidemia
E78.4Other hyperlipidemia
E78.5Hyperlipidemia, unspecified
E78.6Lipoprotein deficiency
E78.7Disorders of bile acid and cholesterol metabolism
E78.70Disorder of bile acid and cholesterol metabolism, unspecified
E78.71Barth syndrome
E78.72Smith-Lemli-Opitz syndrome
E78.79Other disorders of bile acid and cholesterol metabolism
E78.8Other disorders of lipoprotein metabolism
E78.81Lipoid dermatoarthritis
E78.89Other lipoprotein metabolism disorders
E78.9Disorder of lipoprotein metabolism, unspecified
E79Disorders of purine and pyrimidine metabolism
E79.0Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
E79.1Lesch-Nyhan syndrome
E79.2Myoadenylate deaminase deficiency
E79.8Other disorders of purine and pyrimidine metabolism
E79.9Disorder of purine and pyrimidine metabolism, unspecified
E80Disorders of porphyrin and bilirubin metabolism
E80.0Hereditary erythropoietic porphyria
E80.1Porphyria cutanea tarda
E80.2Other and unspecified porphyria
E80.20Unspecified porphyria
E80.21Acute intermittent (hepatic) porphyria
E80.29Other porphyria
E80.3Defects of catalase and peroxidase
E80.4Gilbert syndrome
E80.5Crigler-Najjar syndrome
E80.6Other disorders of bilirubin metabolism
E80.7Disorder of bilirubin metabolism, unspecified
E83Disorders of mineral metabolism
E83.0Disorders of copper metabolism
E83.00Disorder of copper metabolism, unspecified
E83.01Wilson's disease
E83.09Other disorders of copper metabolism
E83.1Disorders of iron metabolism
E83.10Disorder of iron metabolism, unspecified
E83.110Hereditary hemochromatosis
E83.111Hemochromatosis due to repeated red blood cell transfusions
E83.118Other hemochromatosis
E83.119Hemochromatosis, unspecified
E83.19Other disorders of iron metabolism
E83.2Disorders of zinc metabolism
E83.3Disorders of phosphorus metabolism and phosphatases
E83.30Disorder of phosphorus metabolism, unspecified
E83.31Familial hypophosphatemia
E83.32Hereditary vitamin D-dependent rickets (type 1) (type 2)
E83.39Other disorders of phosphorus metabolism
E83.4Disorders of magnesium metabolism
E83.40Disorders of magnesium metabolism, unspecified
E83.49Other disorders of magnesium metabolism
E83.5Disorders of calcium metabolism
E83.50Unspecified disorder of calcium metabolism
E83.59Other disorders of calcium metabolism
E83.8Other disorders of mineral metabolism
E83.81Hungry bone syndrome
E83.89Other disorders of mineral metabolism
E83.9Disorder of mineral metabolism, unspecified
E84Cystic fibrosis
E84.0Cystic fibrosis with pulmonary manifestations
E84.1Cystic fibrosis with intestinal manifestations
E84.11Meconium ileus in cystic fibrosis
E84.19Cystic fibrosis with other intestinal manifestations
E84.8Cystic fibrosis with other manifestations
E84.9Cystic fibrosis, unspecified
E85.0Non-neuropathic heredofamilial amyloidosis
E85.1Neuropathic heredofamilial amyloidosis
E85.2Heredofamilial amyloidosis, unspecified
E85.3Secondary systemic amyloidosis
E85.4Organ-limited amyloidosis
E85.8Other amyloidosis
E85.9Amyloidosis, unspecified
E86Volume depletion
E86.9Volume depletion, unspecified
E87Other disorders of fluid, electrolyte and acid-base balance
E87.0Hyperosmolality and hypernatremia
E87.1Hypo-osmolality and hyponatremia
E87.4Mixed disorder of acid-base balance
E87.7Fluid overload
E87.70Fluid overload, unspecified
E87.71Transfusion associated circulatory overload
E87.79Other fluid overload
E87.8Other disorders of electrolyte and fluid balance, not elsewhere classified
E88Other and unspecified metabolic disorders
E88.0Disorders of plasma-protein metabolism, not elsewhere classified
E88.01Alpha-1-antitrypsin deficiency
E88.09Other disorders of plasma-protein metabolism, not elsewhere classified
E88.1Lipodystrophy, not elsewhere classified
E88.2Lipomatosis, not elsewhere classified
E88.3Tumor lysis syndrome
E88.4Mitochondrial metabolism disorders
E88.40Mitochondrial metabolism disorder, unspecified
E88.41MELAS syndrome
E88.42MERRF syndrome
E88.49Other mitochondrial metabolism disorders
E88.8Other specified metabolic disorders
E88.81Metabolic syndrome
E88.89Other specified metabolic disorders
E88.9Metabolic disorder, unspecified