G60.8 OTHER HEREDITARY AND IDIOPATHIC NEUROPATHIES

Synonyms

• Acute sensory polyneuropathy
• Akinesia
• Andermann syndrome
• Autosomal dominant distal hereditary motor neuropathy
• Autosomal dominant sensory neuropathy
• Autosomal recessive axonal neuropathy with neuromyotonia
• Axonal neuropathy
• Axonal neuropathy
• Axonal neuropathy
• Body height below reference range
• Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
• CLCN6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome
• Congenital anosmia
• Congenital insensitivity to pain with severe intellectual disability
• Congenital insensitivity to pain, anosmia, neuropathic arthropathy
• Congenital insensitivity to pain, hyperhidrosis, absence of cutaneous sensory innervation
• Congenital sensory neuropathy with selective loss of small myelinated fibers
• Deafness-dystonia-optic neuronopathy syndrome
• Disorder of smell
• 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 6
• 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
• Loss of sense of smell
• Mitchell syndrome
• Mixed sensory-motor polyneuropathy
• Morvan syndrome
• Motor polyneuropathy
• Neuromyotonia
• Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy
• Ocular anomalies, axonal neuropathy, developmental delay syndrome
• Parkinsonism with polyneuropathy
• Peripheral axonal neuropathy
• Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
• Polyendocrine polyneuropathy syndrome
• Second cranial nerve finding
• Sensory neuropathy
• Sensory neuropathy
• Sensory neuropathy
• Sensory neuropathy
• Sensory polyneuropathy
• 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

Crosswalk Information

ICD-10 Code		ICD-9 Code	ICD-9 Description
G60.8		356.8	Idio periph neurpthy NEC

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