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