277.86 - Peroxisomal Disorders

The ICD 9 Code for Peroxisomal disorders is listed as 277.86.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.

ICD 9 CM Field	Value
Diagnosis Code:	277.86
Long Description:	Peroxisomal disorders
Short Description:	Peroxisomal disorders

Chapter:	Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders
Block:	Other Metabolic Disorders And Immunity Disorders (270-279)
ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD-10-CM Code:	E71.50 - Peroxisomal disorder, unspecified (approximate)
ICD-10-CM Code:	E71.510 - Zellweger syndrome (approximate)
ICD-10-CM Code:	E71.511 - Neonatal adrenoleukodystrophy (approximate)
ICD-10-CM Code:	E71.522 - Adrenomyeloneuropathy (approximate)
ICD-10-CM Code:	E71.529 - X-linked adrenoleukodystrophy, unspecified type (approximate)
ICD-10-CM Code:	E71.548 - Other peroxisomal disorders (approximate)
ICD-9-CM Siblings (same level / similar specificity) of 277.86:
277.81 - Primary carnitine deficiency
277.82 - Carnitine deficiency due to inborn errors of metabolism
277.83 - Iatrogenic carnitine deficiency
277.84 - Other secondary carnitine deficiency
277.85 - Disorders of fatty acid oxidation
277.87 - Disorders of mitochondrial metabolism
277.88 - Tumor lysis syndrome
277.89 - Other specified disorders of metabolism