G60.1
BillableRefsum's disease
Refsum's disease
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Infantile Refsum disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(5)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(188)
SNOMED CT
- Dilated cardiomyopathy due to phytanic acid storage disease11104006
- Dilated cardiomyopathy secondary to Refsum disease11104006
- Dilated cardiomyopathy secondary to Refsum's disease11104006
- Dilated cardiomyopathy secondary to phytanic acid storage disease11104006
- HSMN IV25362006
- Hereditary motor and sensory neuropathy type IV25362006
- Hereditary motor and sensory neuropathy, type IV25362006
- Hereditary sensory-motor neuropathy, type IV25362006
- Heredoataxia hemeralopica polyneuritiformis25362006
- Heredoataxic atactica polyneuritiformis25362006
- Heredoataxic hemeralopica polyneuritiformis25362006
- Heredopathia atactica polyneuritiformis25362006
- Phytanic acid storage disease25362006
- Refsum syndrome25362006
- Refsum's disease25362006
- Refsum-Thiebaut disease25362006
- Refsum-Thiébaut disease25362006
- Dilated cardiomyopathy due to metabolic disorder111285003
- Dilated cardiomyopathy secondary to metabolic disorder111285003
- Metabolic cardiomyopathy111285003
- Infantile Refsum disease238062008
- Infantile Refsum's disease238062008
- Loss of multiple peroxisomal functions238063003
- Pseudoinfantile Refsum disease238065005
- Pseudoinfantile Refsum's disease238065005
- Ataxia co-occurrent and due to phytanic acid storage disease724769002
- Ataxia with Refsum disease724769002
- Autonomic neuropathy due to Refsum Disease838347009
- Autonomic neuropathy due to Refsum's Disease838347009
- Cardiomyopathy due to storage disease860839005
- Ophthalmoplegia due to neuropathy1231203009
- Ophthalmoplegia due to hereditary motor and sensory neuropathy type IV1231683004
- Ophthalmoplegia due to phytanic acid storage disease1231683004
UMLS
- ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATALC0282527
- Disease, Infantile RefsumC0282527
- Disease, Infantile Refsum'sC0282527
- INFANTILE PHYTANIC ACID STORAGE DISC0282527
- INFANTILE PHYTANIC ACID STORAGE DISEASEC0282527
- INFANTILE REFSUM DISC0282527
- INFANTILE REFSUMS DISC0282527
- Infantile Form of Phytanic Acid Storage DiseaseC0282527
- Infantile Phytanic Acid Storage DiseaseC0282527
- Infantile Refsum DiseaseC0282527
- Infantile Refsum diseaseC0282527
- Infantile Refsum's DiseaseC0282527
- Infantile Refsum's diseaseC0282527
- Infantile Refsum's disease (disorder)C0282527
- Infantile Refsums DiseaseC0282527
- PBD1BC0282527
- PEROXISOME BIOGENESIS DISORDER (NALD/IRD)C0282527
- PEROXISOME BIOGENESIS DISORDER (NEONATAL ADRENOLEUKODYSTROPHY/INFANTILE REFSUM DISEASE)C0282527
- PEROXISOME BIOGENESIS DISORDER 1BC0282527
- REFSUM DIS INFANTILEC0282527
- REFSUM DISEASE, INFANTILEC0282527
- REFSUMS DIS INFANTILEC0282527
- Refsum Disease, InfantileC0282527
- Refsum Disease, Infantile FormC0282527
- Refsum's Disease, InfantileC0282527
- Refsums Disease, InfantileC0282527
- infantile refsum diseaseC0282527
- infantile refsum's diseaseC0282527
- ARDC0034960
- Disease, RefsumC0034960
- Disease, Refsum'sC0034960
- HEREDITARY MOTOR AND SENSORY NEUROPATHY IVC0034960
- HEREDOPATHIA ATACTICA POLYNEURITIFORMISC0034960
- HMSN IVC0034960
- HMSN type IVC0034960
- HMSN4C0034960
- HSMN IVC0034960
- Hereditary motor and sensory neuropathy type IVC0034960
- Hereditary motor and sensory neuropathy, type IVC0034960
- Hereditary sensory-motor neuropathy, type IVC0034960
- Heredoataxia hemeralopica polyneuritiformisC0034960
- Heredoataxic atactica polyneuritiformisC0034960
- Heredoataxic hemeralopica polyneuritiformisC0034960
- Heredopathia atactica polyneuritiformisC0034960
- PHYTANIC ACID OXIDASE DEFICIENCYC0034960
- Phytanic acid storage diseaseC0034960
- Phytanic acid storage disease (disorder)C0034960
- REFSUM DISC0034960
- REFSUM DISEASE, CLASSICC0034960
- REFSUMS DISC0034960
- Refsum DiseaseC0034960
- Refsum SyndromeC0034960
- Refsum Thiebaut SyndromeC0034960
- Refsum diseaseC0034960
- Refsum syndromeC0034960
- Refsum's DiseaseC0034960
- Refsum's SyndromeC0034960
- Refsum's diseaseC0034960
- Refsum-Thiebaut SyndromeC0034960
- Refsum-Thiebaut SyndromesC0034960
- Refsum-Thiebaut diseaseC0034960
- Refsum-Thiébaut diseaseC0034960
- Refsums DiseaseC0034960
- Refsums SyndromeC0034960
- Syndrome, RefsumC0034960
- Syndrome, Refsum'sC0034960
- Syndrome, Refsum-ThiebautC0034960
- Syndromes, Refsum-ThiebautC0034960
- disease refsumC0034960
- disease refsum'sC0034960
- disease refsumsC0034960
- heredopathia atactica polyneuritiformisC0034960
- refsum diseaseC0034960
- refsum syndromeC0034960
- refsum's diseaseC0034960
- refsum's syndromeC0034960
- refsums diseaseC0034960
Clinical Terms
- Infantile Refsums Disease
- Ophthalmoplegia due to phytanic acid storage disease
- ARD
- ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL
- Syndromes, Refsum-Thiebaut
- Loss of multiple peroxisomal functions
- REFSUM DISEASE, CLASSIC
- Dilated cardiomyopathy due to phytanic acid storage disease
- Refsum Disease, Infantile
- PEROXISOME BIOGENESIS DISORDER (NEONATAL ADRENOLEUKODYSTROPHY/INFANTILE REFSUM DISEASE)
- refsum disease
- REFSUM DIS
- Dilated cardiomyopathy secondary to phytanic acid storage disease
- disease refsums
- Ophthalmoplegia due to neuropathy
- Infantile Form of Phytanic Acid Storage Disease
- Phytanic acid storage disease
- Pseudoinfantile Refsum disease
- Autonomic neuropathy due to Refsum's Disease
- Syndrome, Refsum-Thiebaut
- Refsum Syndrome
- Heredoataxic atactica polyneuritiformis
- HMSN4
- PBD1B
- REFSUMS DIS
- Refsum-Thiebaut Syndromes
- Refsums Disease
- Infantile Refsum disease
- HSMN IV
- Refsum Disease, Infantile Form
- Dilated cardiomyopathy secondary to Refsum disease
- HMSN type IV
- Phytanic acid storage disease (disorder)
- INFANTILE PHYTANIC ACID STORAGE DIS
- Heredoataxic hemeralopica polyneuritiformis
- REFSUM DIS INFANTILE
- Refsums Disease, Infantile
- HEREDOPATHIA ATACTICA POLYNEURITIFORMIS
- Refsum's Disease, Infantile
- Dilated cardiomyopathy due to metabolic disorder
- Disease, Infantile Refsum
- Syndrome, Refsum
- Pseudoinfantile Refsum's disease
- Disease, Infantile Refsum's
- Infantile Refsum's Disease
- HEREDITARY MOTOR AND SENSORY NEUROPATHY IV
- Ophthalmoplegia due to hereditary motor and sensory neuropathy type IV
- Ataxia co-occurrent and due to phytanic acid storage disease
- Dilated cardiomyopathy secondary to Refsum's disease
- Hereditary sensory-motor neuropathy, type IV
- Cardiomyopathy due to storage disease
- REFSUMS DIS INFANTILE
- Autonomic neuropathy due to Refsum Disease
- Metabolic cardiomyopathy
- INFANTILE REFSUMS DIS
- Syndrome, Refsum's
- disease refsum
- Disease, Refsum
- Disease, Refsum's
- Refsum-Thiebaut Syndrome
- Refsum Thiebaut Syndrome
- HMSN IV
- refsum's syndrome
- Infantile Refsum's disease (disorder)
- PEROXISOME BIOGENESIS DISORDER 1B
- Dilated cardiomyopathy secondary to metabolic disorder
- Refsum-Thiébaut disease
- Refsum-Thiebaut disease
- Refsums Syndrome
- Heredoataxia hemeralopica polyneuritiformis
- INFANTILE REFSUM DIS
- Ataxia with Refsum disease
- PEROXISOME BIOGENESIS DISORDER (NALD/IRD)
- PHYTANIC ACID OXIDASE DEFICIENCY
- Infantile Phytanic Acid Storage Disease
- disease refsum's
- Hereditary motor and sensory neuropathy, type IV
- Hereditary motor and sensory neuropathy type IV
Frequently Asked Questions
What is the ICD-10 code for refsum's disease?
The ICD-10-CM code for refsum's disease is G60.1. The full clinical description is "Refsum's disease". G60.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G60.1 mean?
ICD-10-CM code G60.1 represents “Refsum's disease”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G60.1 a billable code?
Yes, G60.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G60.1 in?
G60.1 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G60.1?
G60.1 has Excludes1 notes indicating codes that cannot be used together with it, including: neuralgia NOS (M79.2); neuritis NOS (M79.2); peripheral neuritis in pregnancy (O26.82-); and 1 more.
What SNOMED CT codes does G60.1 map to?
G60.1 maps to 11 SNOMED CT concepts: 724769002, 838347009, 860839005, 111285003, 11104006, and 6 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G60.1?
G60.1 is linked to 2 UMLS Concept Unique Identifiers: C0282527, C0034960. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G60.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like refsum's disease affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of G60.1?
G60.1 maps to the ICD-11 code: 5C57.1 (Disorders of peroxisomal alpha-, beta- or omega-oxidation).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.