Billable/Specific ICD-10-CM Codes - Page 36

There are 35,750 ICD-10-CM codes which are billable/specific and can be used to indicate a diagnosis for reimbursement purposes as there are no codes with a greater level of specificity under each code.

  • E66.01 - Morbid (severe) obesity due to excess calories
  • E66.09 - Other obesity due to excess calories
  • E66.1 - Drug-induced obesity
  • E66.2 - Morbid (severe) obesity with alveolar hypoventilation
  • E66.3 - Overweight
  • E66.811 - Obesity, class 1
  • E66.812 - Obesity, class 2
  • E66.813 - Obesity, class 3
  • E66.89 - Other obesity not elsewhere classified
  • E66.9 - Obesity, unspecified
  • E67.0 - Hypervitaminosis A
  • E67.1 - Hypercarotenemia
  • E67.2 - Megavitamin-B6 syndrome
  • E67.3 - Hypervitaminosis D
  • E67.8 - Other specified hyperalimentation
  • E70.0 - Classical phenylketonuria
  • E70.1 - Other hyperphenylalaninemias
  • E70.20 - Disorder of tyrosine metabolism, unspecified
  • E70.21 - Tyrosinemia
  • E70.29 - Other disorders of tyrosine metabolism
  • E70.30 - Albinism, unspecified
  • E70.310 - X-linked ocular albinism
  • E70.311 - Autosomal recessive ocular albinism
  • E70.318 - Other ocular albinism
  • E70.319 - Ocular albinism, unspecified
  • E70.320 - Tyrosinase negative oculocutaneous albinism
  • E70.321 - Tyrosinase positive oculocutaneous albinism
  • E70.328 - Other oculocutaneous albinism
  • E70.329 - Oculocutaneous albinism, unspecified
  • 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
  • E70.40 - Disorders of histidine metabolism, unspecified
  • E70.41 - Histidinemia
  • E70.49 - Other disorders of histidine metabolism
  • E70.5 - Disorders of tryptophan 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
  • E71.0 - Maple-syrup-urine disease
  • E71.110 - Isovaleric acidemia
  • E71.111 - 3-methylglutaconic aciduria
  • E71.118 - Other branched-chain organic acidurias
  • 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
  • E71.30 - Disorder of fatty-acid metabolism, unspecified
  • 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
  • E71.40 - 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
  • E71.440 - Ruvalcaba-Myhre-Smith syndrome
  • E71.448 - Other secondary carnitine deficiency
  • E71.50 - Peroxisomal disorder, unspecified
  • E71.510 - Zellweger syndrome
  • E71.511 - Neonatal adrenoleukodystrophy
  • E71.518 - Other disorders of peroxisome biogenesis
  • 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
  • E71.540 - Rhizomelic chondrodysplasia punctata
  • E71.541 - Zellweger-like syndrome
  • E71.542 - Other group 3 peroxisomal disorders
  • E71.548 - Other peroxisomal disorders
  • 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
  • E72.10 - 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
  • E72.20 - 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
  • E72.50 - Disorder of glycine metabolism, unspecified
  • E72.51 - Non-ketotic hyperglycinemia
  • E72.52 - Trimethylaminuria
  • E72.53 - Primary hyperoxaluria