Other specified and unspecified nutritional and metabolic disorders

Code Families in This Category

• E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism · 38
• E72 Other disorders of amino-acid metabolism · 33
• E83 Disorders of mineral metabolism · 31
• E70 Disorders of aromatic amino-acid metabolism · 27
• E75 Disorders of sphingolipid metabolism and other lipid storage disorders · 26
• E88 Other and unspecified metabolic disorders · 26
• E74 Other disorders of carbohydrate metabolism · 25
• E76 Disorders of glycosaminoglycan metabolism · 12
• E80 Disorders of porphyrin and bilirubin metabolism · 10
• E85 Amyloidosis · 10
• D81 Combined immunodeficiencies · 9
• E78 Disorders of lipoprotein metabolism and other lipidemias · 8
• E79 Disorders of purine and pyrimidine metabolism · 8
• E67 Other hyperalimentation · 5
• E73 Lactose intolerance · 4
• E77 Disorders of glycoprotein metabolism · 4
• E65 Localized adiposity · 1
• E66 Overweight and obesity · 1
• P09 Abnormal findings on neonatal screening · 1

ICD-10-CM Codes in This Category (first 100 of 279)

• D81.3 — Adenosine deaminase [ADA] deficiency
• D81.30 — Adenosine deaminase deficiency, unspecified
• D81.31 — Severe combined immunodeficiency due to adenosine deaminase deficiency
• D81.32 — Adenosine deaminase 2 deficiency
• D81.39 — Other adenosine deaminase deficiency
• D81.5 — Purine nucleoside phosphorylase [PNP] deficiency
• D81.810 — Biotinidase deficiency
• D81.818 — Other biotin-dependent carboxylase deficiency
• D81.819 — Biotin-dependent carboxylase deficiency, unspecified
• E65 — Localized adiposity
• E66.3 — Overweight
• 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
• E70.8 — 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
• 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

The remaining 179 codes are reachable through the code families above.