AutoICD API

G60.8

Billable

Other hereditary and idiopathic neuropathies

Other hereditary and idiopathic neuropathies

Status

Billable / Specific

Block

G60-G65

Parent Code

G60

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

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

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

Related Codes(5)
G60.0

Hereditary motor and sensory neuropathy

BillableG60.1

Refsum's disease

BillableG60.2

Neuropathy in association with hereditary ataxia

BillableG60.3

Idiopathic progressive neuropathy

BillableG60.9

Hereditary and idiopathic neuropathy, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

8C4ZDisorders of nerve root, plexus or peripheral nerves, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(309)

SNOMED CT

UMLS

Clinical Terms

  • Recessively inherited sensory neuropathy
  • Axonal neuropathy
  • Dominantly inherited sensory neuropathy
  • Familial episodic pain syndrome
  • Facial onset sensory and motor neuronopathy syndrome
  • Congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction
  • Small nerve fiber neuropathy
  • Hereditary insensitivity to pain with anhidrosis
  • Autosomal recessive axonal neuropathy with neuromyotonia
  • Sodium channelopathy-related small fiber neuropathy
  • Absent smell
  • Peripheral axonal neuropathy
  • FEPS - familial episodic pain syndrome
  • Hereditary sensory and autonomic neuropathy due to TECPR2 (tectonin beta-propeller repeat containing 2) mutation
  • Waardenburg syndrome
  • HSAN V
  • Autosomal dominant sensory neuropathy
  • Congenital insensitivity to pain with severe intellectual disability
  • X-linked recessive sensory neuropathy
  • Small fiber neuropathy
  • Congenital anosmia
  • Hereditary sensory and autonomic neuropathy type 8
  • Sensory neuropathy
  • HSAN IV
  • Hereditary sensory and autonomic neuropathy type V
  • Sodium channelopathy-related small fibre neuropathy
  • Ocular anomalies, axonal neuropathy, developmental delay syndrome
  • Congenital sensory neuropathy with selective loss of small myelinated fibers
  • Mixed sensory-motor polyneuropathy
  • Congenital insensitivity to pain with severe non-progressive cognitive delay
  • Disorder of smell
  • Akinesia
  • Andermann syndrome
  • Second cranial nerve finding
  • Harel Yoon syndrome
  • Congenital sensory neuropathy with selective loss of small myelinated fibres
  • SFNP - Small fiber neuropathy
  • HSAN8 - hereditary sensory and autonomic neuropathy type 8
  • Hereditary sensory and autonomic neuropathy, type V
  • X-linked auditory neuropathy with peripheral sensory neuropathy type 1
  • morvan's disease
  • CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
  • Hereditary sensory and autonomic neuropathy with spastic paraplegia
  • Morvan fibrillary chorea
  • Chloride voltage-gated channel 6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome
  • MORVAN DISEASE
  • Hypomyelination neuropathy arthrogryposis syndrome
  • No sense of smell
  • Congenital analgesia with hyperhidrosis
  • Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndrome
  • Neurologic Waardenburg Shah syndrome
  • CLCN6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome
  • Painless whitlow disease
  • Hereditary sensory and autonomic neuropathy type II
  • Nelaton's syndrome
  • Myokymia, myotonia and muscle wasting
  • Sense of smell absent
  • Hereditary sensory and autonomic neuropathy type 6
  • Hereditary sensory-motor neuropathy type V
  • Autosomal dominant distal hereditary motor neuropathy
  • Neuromyotonia
  • Anosmia (loss of sense of smell)
  • Sense of smell lost
  • Sodium voltage-gated channel alpha subunit 9-related congenital insensitivity to pain
  • Giant axonal neuropathy
  • Charcot-Marie-Tooth disease, pyramidal features syndrome
  • Congenital analgesia with severe intellectual disability
  • Congenital insensitivity to pain, anhidrosis and mental retardation
  • Hereditary sensory autonomic neuropathy type IIC
  • HSAN6 - hereditary sensory and autonomic neuropathy type 6
  • Hereditary sensory and autonomic neuropathy type VI
  • Loss of sense of smell
  • Autosomal recessive neuromyotonia with axonal neuropathy
  • Polyendocrine polyneuropathy syndrome
  • Congenital insensitivity to pain, anosmia, neuropathic arthropathy
  • FOSMN syndrome
  • Deafness-dystonia-optic neuronopathy syndrome
  • Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy
  • Congenital absence of pain with hyperhidrosis
  • Morvan Diseases
  • Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy
  • Charlevoix disease
  • Familial dysautonomia with contractures
  • Hereditary sensory neuropathy
  • Deafness-dystonia syndrome
  • Congenital indifference to pain with hyperhidrosis
  • PEPNS - polyendocrine polyneuropathy syndrome
  • Dominant hereditary sensory neuropathy, type II
  • Body height below reference range
  • Autosomal recessive hereditary sensory neuropathy
  • FOSMN (facial onset sensory and motor neuronopathy) syndrome
  • Hereditary sensory and autonomic neuropathy type IV
  • Hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction
  • Posterior sensory radicular neuropathy
  • Congenital insensitivity to pain, hyperhidrosis, absence of cutaneous sensory innervation
  • Waardenburg's syndrome
  • Antinolo Nieto Borrego syndrome
  • Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
  • Hereditary sensory and autonomic neuropathy type 7
  • Hereditary sensory and autonomic neuropathy type VIII
  • X-linked hereditary sensory and autonomic neuropathy with deafness
  • HSAN - hereditary sensory and autonomic neuropathy
  • Congenital sensory neuropathy with anhidrosis
  • Distal hereditary motor neuropathy type 2
  • Motor polyneuropathy
  • Swanson-Buchanan-Alvord neuropathy syndrome
  • Continuous muscle fiber activity
  • Morvan syndrome
  • Morvan's Diseases
  • Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder
  • Sensory polyneuropathy
  • Autosomal dominant distal spinal muscular atrophy type 2
  • Parkinsonism with polyneuropathy
  • SCN9A-related congenital insensitivity to pain
  • Hereditary sensory and autonomic neuropathy, type II
  • Anosmia
  • SPOAN and SPOAN-related disorder
  • Small fibre neuropathy
  • Congenital absence of pain with severe intellectual disability
  • Continuous muscle fibre activity
  • HSAN7- hereditary sensory and autonomic neuropathy type 7
  • Hereditary sensory and autonomic neuropathy
  • Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
  • Idiopathic small fibre peripheral neuropathy
  • Loss of the sense of smell
  • MORVAN DIS
  • Autosomal recessive spastic paraplegia type 49
  • Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation
  • Mitchell syndrome
  • Hereditary motor and sensory neuropathy type 5
  • Morvans Disease
  • PCWH - peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
  • Acute sensory polyneuropathy
  • Hereditary growth hormone deficiency
  • Hereditary sensory and autonomic neuropathy type VII
  • Symmetrical sensory neuropathy
  • X-linked HSAN (hereditary sensory and autonomic neuropathy) with deafness
  • Congenital insensitivity to pain with preserved temperature sensation
  • Gamstorp-Wohlfart syndrome
  • Morvan syndrome (disorder)
  • Congenital insensitivity to pain with hyperhidrosis
  • HSAN (hereditary sensory and autonomic neuropathy) with spastic paraplegia
  • Agenesis of corpus callosum with polyneuropathy
  • Hereditary sensory and autonomic neuropathy due to TECPR2 mutation
  • Idiopathic small fiber peripheral neuropathy
  • Optic nerve finding
  • Spastic paraplegia, neuropathy, poikiloderma syndrome
  • Mohr-Tranebjaerg syndrome
  • Hereditary sensory and autonomic neuropathy, type IV
  • Agenesis of corpus callosum with peripheral neuropathy
Frequently Asked Questions
What is the ICD-10 code for other hereditary and idiopathic neuropathies?

The ICD-10-CM code for other hereditary and idiopathic neuropathies is G60.8. The full clinical description is "Other hereditary and idiopathic neuropathies". G60.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G60.8 mean?

ICD-10-CM code G60.8 represents “Other hereditary and idiopathic neuropathies”. 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 G60.8 a billable code?

Yes, G60.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is G60.8 in?

G60.8 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).

What codes cannot be used with G60.8?

G60.8 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 G60.8 map to?

G60.8 maps to 58 SNOMED CT concepts: 44169009, 1259063005, 702439002, 33994004, 763402002, and 53 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for G60.8?

G60.8 is linked to 5 UMLS Concept Unique Identifiers: C2875301, C3854373, C2875302, C0477392, C2875303. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does G60.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other hereditary and idiopathic neuropathies 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 G60.8?

G60.8 maps to the ICD-11 code: 8C4Z (Disorders of nerve root, plexus or peripheral nerves, unspecified).

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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.