Browse all the diagnosis codes used for metabolic disorders (e70-e88). For easy navigation, the diagnosis codes are sorted in alphabetical order and grouped by sections. Each section is clearly marked with its description, and the corresponding three-digit code range. This format makes it simple to browse diagnosis codes in this chapter or section and find what you're looking for. We've also added green checkmark icons to label billable codes, and red warning icons for non-billable ones. This makes it easy to identify which codes can be billed.
Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
androgen insensitivity syndrome E34.5 congenital adrenal hyperplasia E25.0 hemolytic anemias attributable to enzyme disorders D55 Marfan syndrome Q87.4 5-alpha-reductase deficiency E29.1
Type 2 Excludes
A type 2 excludes note represents "Not included here". An excludes2 note indicates that the condition excluded is not part of the condition represented by the code, but a patient may have both conditions at the same time. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate.
Ehlers-Danlos syndromes Q79.6
Filter diagnosis codes list: Endocrine, nutritional and metabolic diseases (E00–E89) Metabolic disorders (E70-E88) Disorders of aromatic amino-acid metabolism (E70) E70 Disorders of aromatic amino-acid metabolism E70.0 Classical phenylketonuria E70.1 Other hyperphenylalaninemias E70.2 Disorders of tyrosine metabolism E70.20 Disorder of tyrosine metabolism, unspecified E70.21 Tyrosinemia E70.29 Other disorders of tyrosine metabolism E70.30 Albinism, unspecified E70.31 Ocular albinism E70.310 X-linked ocular albinism E70.311 Autosomal recessive ocular albinism E70.318 Other ocular albinism E70.319 Ocular albinism, unspecified E70.32 Oculocutaneous albinism E70.320 Tyrosinase negative oculocutaneous albinism E70.321 Tyrosinase positive oculocutaneous albinism E70.328 Other oculocutaneous albinism E70.329 Oculocutaneous albinism, unspecified E70.33 Albinism with hematologic abnormality E70.330 Chediak-Higashi syndrome E70.331 Hermansky-Pudlak syndrome E70.338 Other albinism with hematologic abnormality E70.339 Albinism with hematologic abnormality, unspecified E70.39 Other specified albinism E70.4 Disorders of histidine metabolism E70.40 Disorders of histidine metabolism, unspecified E70.41 Histidinemia E70.49 Other disorders of histidine metabolism E70.5 Disorders of tryptophan metabolism E70.8 Other disorders of aromatic amino-acid metabolism E70.81 Aromatic L-amino acid decarboxylase deficiency E70.89 Other disorders of aromatic amino-acid metabolism E70.9 Disorder of aromatic amino-acid metabolism, unspecified Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism (E71) E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism E71.0 Maple-syrup-urine disease E71.1 Other disorders of branched-chain amino-acid metabolism E71.11 Branched-chain organic acidurias E71.110 Isovaleric acidemia E71.111 3-methylglutaconic aciduria E71.118 Other branched-chain organic acidurias E71.12 Disorders of propionate metabolism E71.120 Methylmalonic acidemia E71.121 Propionic acidemia E71.128 Other disorders of propionate metabolism E71.19 Other disorders of branched-chain amino-acid metabolism E71.2 Disorder of branched-chain amino-acid metabolism, unspecified E71.3 Disorders of fatty-acid metabolism E71.30 Disorder of fatty-acid metabolism, unspecified E71.31 Disorders of fatty-acid oxidation E71.310 Long chain/very long chain acyl CoA dehydrogenase deficiency E71.311 Medium chain acyl CoA dehydrogenase deficiency E71.312 Short chain acyl CoA dehydrogenase deficiency E71.313 Glutaric aciduria type II 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 E71.40 Disorder of carnitine metabolism, unspecified E71.41 Primary carnitine deficiency E71.42 Carnitine deficiency due to inborn errors of metabolism E71.43 Iatrogenic carnitine deficiency E71.44 Other secondary carnitine deficiency E71.440 Ruvalcaba-Myhre-Smith syndrome E71.448 Other secondary carnitine deficiency E71.5 Peroxisomal disorders E71.50 Peroxisomal disorder, unspecified E71.51 Disorders of peroxisome biogenesis E71.510 Zellweger syndrome E71.511 Neonatal adrenoleukodystrophy E71.518 Other disorders of peroxisome biogenesis E71.52 X-linked adrenoleukodystrophy E71.520 Childhood cerebral X-linked adrenoleukodystrophy E71.521 Adolescent X-linked adrenoleukodystrophy E71.522 Adrenomyeloneuropathy E71.528 Other X-linked 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 E71.541 Zellweger-like syndrome E71.542 Other group 3 peroxisomal disorders E71.548 Other peroxisomal disorders Other disorders of amino-acid metabolism (E72) E72 Other disorders of amino-acid metabolism E72.0 Disorders of amino-acid transport E72.00 Disorders of amino-acid transport, unspecified E72.01 Cystinuria E72.02 Hartnup's disease E72.03 Lowe's syndrome E72.04 Cystinosis E72.09 Other disorders of amino-acid transport E72.1 Disorders of sulfur-bearing amino-acid metabolism E72.10 Disorders of sulfur-bearing amino-acid metabolism, unspecified E72.11 Homocystinuria E72.12 Methylenetetrahydrofolate reductase deficiency E72.19 Other disorders of sulfur-bearing amino-acid metabolism E72.2 Disorders of urea cycle metabolism E72.20 Disorder of urea cycle metabolism, unspecified E72.21 Argininemia E72.22 Arginosuccinic aciduria E72.23 Citrullinemia E72.29 Other disorders of urea cycle metabolism E72.3 Disorders of lysine and hydroxylysine metabolism E72.4 Disorders of ornithine metabolism E72.5 Disorders of glycine metabolism E72.50 Disorder of glycine metabolism, unspecified E72.51 Non-ketotic hyperglycinemia E72.52 Trimethylaminuria E72.53 Primary hyperoxaluria E72.59 Other disorders of glycine metabolism E72.8 Other specified disorders of amino-acid metabolism E72.81 Disorders of gamma aminobutyric acid metabolism E72.89 Other specified disorders of amino-acid metabolism E72.9 Disorder of amino-acid metabolism, unspecified Other disorders of carbohydrate metabolism (E74) E74 Other disorders of carbohydrate metabolism E74.0 Glycogen storage disease E74.00 Glycogen storage disease, unspecified E74.01 von Gierke disease E74.02 Pompe disease E74.03 Cori disease E74.04 McArdle disease E74.05 Lysosome-associated membrane protein 2 [LAMP2] deficiency NEW CODE E74.09 Other glycogen storage disease E74.1 Disorders of fructose metabolism E74.10 Disorder of fructose metabolism, unspecified E74.11 Essential fructosuria E74.12 Hereditary fructose intolerance E74.19 Other disorders of fructose metabolism E74.2 Disorders of galactose metabolism E74.20 Disorders of galactose metabolism, unspecified E74.21 Galactosemia E74.29 Other disorders of galactose metabolism E74.3 Other disorders of intestinal carbohydrate absorption E74.31 Sucrase-isomaltase deficiency E74.39 Other disorders of intestinal carbohydrate absorption E74.4 Disorders of pyruvate metabolism and gluconeogenesis E74.8 Other specified disorders of carbohydrate metabolism E74.81 Disorders of glucose transport, not elsewhere classified E74.810 Glucose transporter protein type 1 deficiency E74.818 Other disorders of glucose transport E74.819 Disorders of glucose transport, unspecified E74.89 Other specified disorders of carbohydrate metabolism E74.9 Disorder of carbohydrate metabolism, unspecified Disorders of lipoprotein metabolism and other lipidemias (E78) E78 Disorders of lipoprotein metabolism and other lipidemias E78.0 Pure hypercholesterolemia E78.00 Pure hypercholesterolemia, unspecified E78.01 Familial hypercholesterolemia E78.1 Pure hyperglyceridemia E78.2 Mixed hyperlipidemia E78.3 Hyperchylomicronemia E78.4 Other hyperlipidemia E78.41 Elevated Lipoprotein(a) E78.49 Other hyperlipidemia E78.5 Hyperlipidemia, unspecified E78.6 Lipoprotein deficiency E78.7 Disorders of bile acid and cholesterol metabolism E78.70 Disorder of bile acid and cholesterol metabolism, unspecified E78.71 Barth syndrome E78.72 Smith-Lemli-Opitz syndrome E78.79 Other disorders of bile acid and cholesterol metabolism E78.8 Other disorders of lipoprotein metabolism E78.81 Lipoid dermatoarthritis E78.89 Other lipoprotein metabolism disorders E78.9 Disorder of lipoprotein metabolism, unspecified Disorders of purine and pyrimidine metabolism (E79) E79 Disorders of purine and pyrimidine metabolism E79.0 Hyperuricemia without signs of inflammatory arthritis and tophaceous disease E79.1 Lesch-Nyhan syndrome E79.2 Myoadenylate deaminase deficiency E79.8 Other disorders of purine and pyrimidine metabolism NEW CODE E79.81 Aicardi-Goutieres syndrome NEW CODE E79.82 Hereditary xanthinuria NEW CODE E79.89 Other specified disorders of purine and pyrimidine metabolism NEW CODE E79.9 Disorder of purine and pyrimidine metabolism, unspecified Disorders of mineral metabolism (E83) E83 Disorders of mineral metabolism E83.0 Disorders of copper metabolism E83.00 Disorder of copper metabolism, unspecified E83.01 Wilson's disease E83.09 Other disorders of copper metabolism E83.1 Disorders of iron metabolism E83.10 Disorder of iron metabolism, unspecified E83.11 Hemochromatosis E83.110 Hereditary hemochromatosis E83.111 Hemochromatosis due to repeated red blood cell transfusions E83.118 Other hemochromatosis E83.119 Hemochromatosis, unspecified E83.19 Other disorders of iron metabolism E83.2 Disorders of zinc metabolism E83.3 Disorders of phosphorus metabolism and phosphatases E83.30 Disorder of phosphorus metabolism, unspecified E83.31 Familial hypophosphatemia E83.32 Hereditary vitamin D-dependent rickets (type 1) (type 2) E83.39 Other disorders of phosphorus metabolism E83.4 Disorders of magnesium metabolism E83.40 Disorders of magnesium metabolism, unspecified E83.41 Hypermagnesemia E83.42 Hypomagnesemia E83.49 Other disorders of magnesium metabolism E83.5 Disorders of calcium metabolism E83.50 Unspecified disorder of calcium metabolism E83.51 Hypocalcemia E83.52 Hypercalcemia E83.59 Other disorders of calcium metabolism E83.8 Other disorders of mineral metabolism E83.81 Hungry bone syndrome E83.89 Other disorders of mineral metabolism E83.9 Disorder of mineral metabolism, unspecified Cystic fibrosis (E84) E84 Cystic fibrosis E84.0 Cystic fibrosis with pulmonary manifestations E84.1 Cystic fibrosis with intestinal manifestations E84.11 Meconium ileus in cystic fibrosis E84.19 Cystic fibrosis with other intestinal manifestations E84.8 Cystic fibrosis with other manifestations E84.9 Cystic fibrosis, unspecified Amyloidosis (E85) E85 Amyloidosis E85.0 Non-neuropathic heredofamilial amyloidosis E85.1 Neuropathic heredofamilial amyloidosis E85.2 Heredofamilial amyloidosis, unspecified E85.3 Secondary systemic amyloidosis E85.4 Organ-limited amyloidosis E85.8 Other amyloidosis E85.81 Light chain (AL) amyloidosis E85.82 Wild-type transthyretin-related (ATTR) amyloidosis E85.89 Other amyloidosis E85.9 Amyloidosis, unspecified Other and unspecified metabolic disorders (E88) E88 Other and unspecified metabolic disorders E88.0 Disorders of plasma-protein metabolism, not elsewhere classified E88.01 Alpha-1-antitrypsin deficiency E88.02 Plasminogen deficiency E88.09 Other disorders of plasma-protein metabolism, not elsewhere classified E88.1 Lipodystrophy, not elsewhere classified E88.2 Lipomatosis, not elsewhere classified E88.3 Tumor lysis syndrome E88.4 Mitochondrial metabolism disorders E88.40 Mitochondrial metabolism disorder, unspecified E88.41 MELAS syndrome E88.42 MERRF syndrome E88.43 Disorders of mitochondrial tRNA synthetases NEW CODE E88.49 Other mitochondrial metabolism disorders E88.8 Other specified metabolic disorders E88.81 Metabolic syndrome and other insulin resistance NEW CODE E88.810 Metabolic syndrome NEW CODE E88.811 Insulin resistance syndrome, Type A NEW CODE E88.818 Other insulin resistance NEW CODE E88.819 Insulin resistance, unspecified NEW CODE E88.89 Other specified metabolic disorders E88.9 Metabolic disorder, unspecified E88.A Wasting disease (syndrome) due to underlying condition NEW CODE