G60.0Hereditary motor and sensory neuropathy

G60.0 is the ICD-10-CM diagnosis code for hereditary motor and sensory neuropathy. It belongs to category G60 (hereditary and idiopathic neuropathy), block G60-G65 (polyneuropathies and other disorders of the peripheral nervous system) and chapter 6 (diseases of the nervous system). It is billable, so it can be reported on its own for dates of service from October 1, 2026 through September 30, 2027.

Within G60 (hereditary and idiopathic neuropathy), G60.0 is specifically for hereditary motor and sensory neuropathy. Related codes cover Refsum's disease (G60.1), neuropathy in association with hereditary ataxia (G60.2), idiopathic progressive neuropathy (G60.3), other hereditary and idiopathic neuropathies (G60.8) and unspecified (G60.9).

It is not a CC or MCC, so as a secondary diagnosis it doesn't change the MS-DRG severity level.

In MS-DRG v44.0, it is part of the grouping logic for DRG 073 (Cranial and Peripheral Nerve Disorders with MCC, relative weight 1.5779) and DRG 074 (Cranial and Peripheral Nerve Disorders without MCC, relative weight 1.0173), in MDC 01 (Diseases and Disorders of the Nervous System), as a principal or secondary diagnosis. The DRG a claim lands in depends on the principal diagnosis, procedures and any CC/MCC secondary diagnoses.

It has been part of ICD-10-CM since the code set took effect on October 1, 2015 and hasn't changed since.

Before ICD-10, this condition was coded in ICD-9-CM as 356.0 (hereditary peripheral neuropathy), 356.1 (peroneal muscular atrophy) and 356.2 (hereditary sensory neuropathy).