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 period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code G60.1?
ICD-10-CM code G60.1 represents "Refsum's disease". It 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.
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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.