ICD-10-CM codes

97,584 codes · page 97 of 1,952

ICD-10	Description
E7112	Disorders of propionate metabolism
E71120	Methylmalonic acidemia
E71121	Propionic acidemia
E71128	Other disorders of propionate metabolism
E7119	Other disorders of branched-chain amino-acid metabolism
E712	Disorder of branched-chain amino-acid metabolism, unspecified
E713	Disorders of fatty-acid metabolism
E7130	Disorder of fatty-acid metabolism, unspecified
E7131	Disorders of fatty-acid oxidation
E71310	Long chain/very long chain acyl CoA dehydrogenase deficiency Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311	Medium chain acyl CoA dehydrogenase deficiency
E71312	Short chain acyl CoA dehydrogenase deficiency
E71313	Glutaric aciduria type II
E71314	Muscle carnitine palmitoyltransferase deficiency
E71318	Other disorders of fatty-acid oxidation
E7132	Disorders of ketone metabolism
E7139	Other disorders of fatty-acid metabolism
E714	Disorders of carnitine metabolism
E7140	Disorder of carnitine metabolism, unspecified
E7141	Primary carnitine deficiency
E7142	Carnitine deficiency due to inborn errors of metabolism
E7143	Iatrogenic carnitine deficiency
E7144	Other secondary carnitine deficiency
E71440	Ruvalcaba-Myhre-Smith syndrome
E71448	Other secondary carnitine deficiency
E715	Peroxisomal disorders
E7150	Peroxisomal disorder, unspecified
E7151	Disorders of peroxisome biogenesis
E71510	Zellweger syndrome
E71511	Neonatal adrenoleukodystrophy
E71518	Other disorders of peroxisome biogenesis
E7152	X-linked adrenoleukodystrophy
E71520	Childhood cerebral X-linked adrenoleukodystrophy
E71521	Adolescent X-linked adrenoleukodystrophy
E71522	Adrenomyeloneuropathy
E71528	Other X-linked adrenoleukodystrophy
E71529	X-linked adrenoleukodystrophy, unspecified type
E7153	Other group 2 peroxisomal disorders
E7154	Other peroxisomal disorders
E71540	Rhizomelic chondrodysplasia punctata
E71541	Zellweger-like syndrome
E71542	Other group 3 peroxisomal disorders
E71548	Other peroxisomal disorders
E72	Other disorders of amino-acid metabolism
E720	Disorders of amino-acid transport
E7200	Disorders of amino-acid transport, unspecified
E7201	Cystinuria
E7202	Hartnup's disease
E7203	Lowe's syndrome
E7204	Cystinosis

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