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2009 ICD-9-CM
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277.8 Other specified disorders of metabolism | |
 eicd10 | 277.81 Primary carnitine deficiency |
| eicd10 | 277.82 Carnitine deficiency due to inborn errors of metabolism |
| eicd10 | 277.83 Iatrogenic carnitine deficiency
Carnitine deficiency due to:
Hemodialysis
Valproic acid therapy |
| eicd10 | 277.84 Other secondary carnitine deficiency |
| eicd10 | 277.85 Disorders of fatty acid oxidation
Carnitine palmitoyltransferase deficiencies (CPT1, CPT2)
Glutaric aciduria type II (type IIA, IIB, IIC)
Long chain 3-hydroxyacyl CoA dehydrogenase deficiency (LCHAD)
Long chain/very long chain acyl CoA dehydrogenase deficiency (LCAD, VLCAD)
Medium chain acyl CoA dehydrogenase deficiency (MCAD)
Short chain acyl CoA dehydrogenase deficiency (SCAD)
Excludes: primary carnitine deficiency (277.81) |
| eicd10 | 277.86 Peroxisomal disorders
Adrenomyeloneuropathy
Neonatal adrenoleukodystrophy
Rhizomelic chrondrodysplasia punctata
X-linked adrenoleukodystrophy
Zellweger syndrome
Excludes: infantile Refsum disease (356.3) |
| eicd10 | 277.87 Disorders of mitochondrial metabolism
Kearns-Sayre syndrome
Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like episodes (MELAS syndrome)
Mitochondrial Neurogastrointestinal Encephalopathy syndrome (MNGIE)
Myoclonus with Epilepsy and with Ragged Red Fibers (MERRF syndrome)
Neuropathy, Ataxia and Retinitis Pigmentosa (NARP syndrome)
Use additional code for associated conditions
Excludes: disorders of pyruvate metabolism (271.8)
Leber's optic atrophy (377.16)
Leigh's subacute necrotizing encephalopathy (330.8)
Reye's syndrome (331.81) |
| eicd10 | 277.89 Other specified disorders of metabolism
Hand-Schüller-Christian disease
Histiocytosis (acute) (chronic)
Histiocytosis X (chronic)
Excludes: histiocytosis:
acute differentiated progressive (202.5)
X, acute (progressive) (202.5) |