Diagnosis Code: G60.8

Short Description: Other hereditary and idiopathic neuropathies

Long Description: Other hereditary and idiopathic neuropathies

The code G60.8 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Polyneuropathies and other disorders of the peripheral nervous system (G60-G65)
    • Hereditary and idiopathic neuropathy (G60)
      • G60.8 Other hereditary and idiopathic neuropathies

Code Version: 2022 ICD-10-CM

Synonyms

• Acute sensory polyneuropathy
• Akinesia
• Andermann syndrome
• Autosomal dominant complex hereditary spastic paraplegia
• Autosomal dominant distal hereditary motor neuropathy
• Autosomal dominant sensory neuropathy
• Autosomal recessive axonal neuropathy with neuromyotonia
• Axonal neuropathy
• Axonal neuropathy
• Axonal neuropathy
• Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
• Congenital insensitivity to pain with severe intellectual disability
• Congenital sensory neuropathy with selective loss of small myelinated fibers
• Deafness-dystonia-optic neuronopathy syndrome
• Distal hereditary motor neuropathy type 2
• Facial onset sensory and motor neuronopathy syndrome
• Familial episodic pain syndrome
• Giant axonal neuropathy
• Hereditary growth hormone deficiency
• Hereditary insensitivity to pain with anhidrosis
• Hereditary motor and sensory neuropathy type 5
• Hereditary sensory and autonomic neuropathy
• Hereditary sensory and autonomic neuropathy due to TECPR2 mutation
• Hereditary sensory and autonomic neuropathy type 7
• Hereditary sensory and autonomic neuropathy type 8
• Hereditary sensory and autonomic neuropathy type II
• Hereditary sensory and autonomic neuropathy with spastic paraplegia
• Hereditary sensory autonomic neuropathy type IIC
• Hereditary sensory neuropathy
• Hereditary sensory neuropathy
• Hypomyelination neuropathy arthrogryposis syndrome
• Idiopathic small fiber peripheral neuropathy
• Morvan syndrome
• Neuromyotonia
• Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy
• Ocular anomalies, axonal neuropathy, developmental delay syndrome
• Peripheral axonal neuropathy
• Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
• Second cranial nerve finding
• Sensory neuropathy
• Sensory neuropathy
• Sensory neuropathy
• Sensory neuropathy
• Sensory polyneuropathy
• Small fiber neuropathy
• Small fiber neuropathy
• Sodium channelopathy-related small fiber neuropathy
• Spastic paraplegia, neuropathy, poikiloderma syndrome
• SPOAN and SPOAN-related disorder
• Symmetrical sensory neuropathy
• Waardenburg syndrome
• X-linked hereditary sensory and autonomic neuropathy with deafness
• X-linked recessive sensory neuropathy

References to Index of Diseases and Injuries

The code G60.8 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Dominantly inherited sensory neuropathy
  • Morvan's disease
  • Nelaton's syndrome
  • Recessively inherited sensory neuropathy

Crosswalk Information

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This page was last updated on: 10/1/2023

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