G60.1 Refsum's disease

Billable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.

Applicable to

• Infantile Refsum disease

MS-DRG index

Defines the logic of DRG(s) 091-093 in MDC 01.

Approximate ICD-9-CM (GEMs)

• 356.3 Refsum's disease

Code annotations containing back-references to G60.1

Back-references to G60.1

• Type 1 Excludes: E71.3 Disorders of fatty-acid metabolism ("Refsum's disease (G60.1)")
• Type 1 Excludes: E71.51 Disorders of peroxisome biogenesis ("Refsum's disease (G60.1)")
• Type 1 Excludes: E72.3 Disorders of lysine and hydroxylysine metabolism ("Refsum's disease (G60.1)")
• Type 1 Excludes: E75 Disorders of sphingolipid metabolism and other lipid storage disorders ("Refsum's disease (G60.1)")
• Type 1 Excludes: Q80 Congenital ichthyosis ("Refsum's disease (G60.1)")

Back-references to G60

• Type 2 Excludes: G11 Hereditary ataxia ("hereditary and idiopathic neuropathy (G60.-)")

Diagnosis Index entries for G60.1

• Disease, diseased › Refsum's (heredopathia atactica polyneuritiformis)
• Heredopathia atactica polyneuritiformis
• Neuropathy, neuropathic › hypertrophic › Refsum
• Polyneuritis, polyneuritic › hereditary ataxic
• Refsum's disease or syndrome
• Syndrome › Refsum's

Nearby codes

• G60 Hereditary and idiopathic neuropathy
• G60.0 Hereditary motor and sensory neuropathy
• G60.1 Refsum's disease (this code)
• G60.2 Neuropathy in association with hereditary ataxia
• G60.3 Idiopathic progressive neuropathy
• G60.8 Other hereditary and idiopathic neuropathies
• G60.9 Hereditary and idiopathic neuropathy, unspecified