G60.8
BillableOther hereditary and idiopathic neuropathies
Other hereditary and idiopathic neuropathies
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
- 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
- Mixed sensory-motor polyneuropathy3900008
- Hereditary sensory neuropathy11442006
- Posterior sensory radicular neuropathy11442006
- Sensory polyneuropathy13694005
- Akinesia33994004
- Absent smell44169009
- Anosmia44169009
- Anosmia (loss of sense of smell)44169009
- Loss of sense of smell44169009
- Loss of the sense of smell44169009
- No sense of smell44169009
- Sense of smell absent44169009
- Sense of smell lost44169009
- Waardenburg syndrome47434006
- Waardenburg's syndrome47434006
- Axonal neuropathy60703000
- Autosomal recessive hereditary sensory neuropathy62985007
- Congenital insensitivity to pain, anhidrosis and mental retardation62985007
- Congenital sensory neuropathy with anhidrosis62985007
- HSAN IV62985007
- Hereditary insensitivity to pain with anhidrosis62985007
- Hereditary sensory and autonomic neuropathy type IV62985007
- Hereditary sensory and autonomic neuropathy, type IV62985007
- Swanson-Buchanan-Alvord neuropathy syndrome62985007
- Motor polyneuropathy85423005
- Sensory neuropathy95662005
- Optic nerve finding106152006
- Second cranial nerve finding106152006
- HSAN - hereditary sensory and autonomic neuropathy128205005
- Hereditary sensory and autonomic neuropathy128205005
- Congenital sensory neuropathy with selective loss of small myelinated fibers128206006
- Congenital sensory neuropathy with selective loss of small myelinated fibres128206006
- HSAN V128206006
- Hereditary sensory and autonomic neuropathy type V128206006
- Hereditary sensory and autonomic neuropathy, type V128206006
- Giant axonal neuropathy128207002
- Peripheral axonal neuropathy128208007
- Congenital anosmia230502003
- Autosomal dominant sensory neuropathy230553002
- X-linked recessive sensory neuropathy230556005
- Disorder of smell275462005
- Continuous muscle fiber activity305719002
- Continuous muscle fibre activity305719002
- Neuromyotonia305719002
- Symmetrical sensory neuropathy309520003
- Dominant hereditary sensory neuropathy, type II398148000
- Hereditary sensory and autonomic neuropathy type II398148000
- Hereditary sensory and autonomic neuropathy, type II398148000
- Painless whitlow disease398148000
- Mohr-Tranebjaerg syndrome702423009
- Deafness-dystonia syndrome702423009
- Deafness-dystonia-optic neuronopathy syndrome702423009
- Agenesis of corpus callosum with peripheral neuropathy702439002
- Agenesis of corpus callosum with polyneuropathy702439002
- Andermann syndrome702439002
- Charlevoix disease702439002
- SFNP - Small fiber neuropathy709489006
- Small fiber neuropathy709489006
- Small fibre neuropathy709489006
- Small nerve fiber neuropathy709489006
- Autosomal recessive axonal neuropathy with neuromyotonia711406009
- Autosomal recessive neuromyotonia with axonal neuropathy711406009
- Gamstorp-Wohlfart syndrome711406009
- Myokymia, myotonia and muscle wasting711406009
- HSAN (hereditary sensory and autonomic neuropathy) with spastic paraplegia717827000
- Hereditary sensory and autonomic neuropathy with spastic paraplegia717827000
- X-linked HSAN (hereditary sensory and autonomic neuropathy) with deafness719838008
- X-linked auditory neuropathy with peripheral sensory neuropathy type 1719838008
- X-linked hereditary sensory and autonomic neuropathy with deafness719838008
- FOSMN (facial onset sensory and motor neuronopathy) syndrome723306004
- FOSMN syndrome723306004
- Facial onset sensory and motor neuronopathy syndrome723306004
- Antinolo Nieto Borrego syndrome763402002
- Spastic paraplegia, neuropathy, poikiloderma syndrome763402002
- Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndrome763803004
- Morvan fibrillary chorea763803004
- Morvan syndrome763803004
- Neurologic Waardenburg Shah syndrome765325002
- PCWH - peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease765325002
- Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease765325002
- Hypomyelination neuropathy arthrogryposis syndrome766931003
- Charcot-Marie-Tooth disease, pyramidal features syndrome771143004
- Hereditary motor and sensory neuropathy type 5771143004
- Hereditary sensory-motor neuropathy type V771143004
- FEPS - familial episodic pain syndrome782756008
- Familial episodic pain syndrome782756008
- Sodium channelopathy-related small fiber neuropathy782824007
- Sodium channelopathy-related small fibre neuropathy782824007
- Autosomal recessive spastic paraplegia type 49783198006
- Hereditary sensory and autonomic neuropathy due to TECPR2 (tectonin beta-propeller repeat containing 2) mutation783198006
- Hereditary sensory and autonomic neuropathy due to TECPR2 mutation783198006
- Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation783198006
- Congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction783550006
- HSAN7- hereditary sensory and autonomic neuropathy type 7783550006
- Hereditary sensory and autonomic neuropathy type 7783550006
- Hereditary sensory and autonomic neuropathy type VII783550006
- Hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction783550006
- SPOAN and SPOAN-related disorder789674008
- Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder789674008
- Autosomal dominant distal hereditary motor neuropathy1156837002
- Harel Yoon syndrome1172586007
- Ocular anomalies, axonal neuropathy, developmental delay syndrome1172586007
- HSAN8 - hereditary sensory and autonomic neuropathy type 81172838005
- Hereditary sensory and autonomic neuropathy type 81172838005
- Hereditary sensory and autonomic neuropathy type VIII1172838005
- Hereditary growth hormone deficiency1186807002
- CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome1220595008
- Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome1220595008
- Non-progressive predominantly posterior cavitating leucodystrophy with peripheral neuropathy1220598005
- Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy1220598005
- Autosomal dominant distal spinal muscular atrophy type 21230343006
- Distal hereditary motor neuropathy type 21230343006
- Congenital absence of pain with severe intellectual disability1237623009
- Congenital analgesia with severe intellectual disability1237623009
- Congenital insensitivity to pain with preserved temperature sensation1237623009
- Congenital insensitivity to pain with severe intellectual disability1237623009
- Congenital insensitivity to pain with severe non-progressive cognitive delay1237623009
- Hereditary sensory autonomic neuropathy type IIC1254941001
- Acute sensory polyneuropathy1259063005
- PEPNS - polyendocrine polyneuropathy syndrome1260449002
- Polyendocrine polyneuropathy syndrome1260449002
- Congenital insensitivity to pain, anosmia, neuropathic arthropathy1279831004
- SCN9A-related congenital insensitivity to pain1279831004
- Sodium voltage-gated channel alpha subunit 9-related congenital insensitivity to pain1279831004
- Congenital absence of pain with hyperhidrosis1279834007
- Congenital analgesia with hyperhidrosis1279834007
- Congenital indifference to pain with hyperhidrosis1279834007
- Congenital insensitivity to pain with hyperhidrosis1279834007
- Congenital insensitivity to pain, hyperhidrosis, absence of cutaneous sensory innervation1279834007
- Familial dysautonomia with contractures1279838005
- HSAN6 - hereditary sensory and autonomic neuropathy type 61279838005
- Hereditary sensory and autonomic neuropathy type 61279838005
- Hereditary sensory and autonomic neuropathy type VI1279838005
- Mitchell syndrome1300194008
- CLCN6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome1340172003
- Chloride voltage-gated channel 6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome1340172003
- Parkinsonism with polyneuropathy1356741005
- Body height below reference range1363478003
- Idiopathic small fiber peripheral neuropathy350471000119102
- Idiopathic small fibre peripheral neuropathy350471000119102
UMLS
- Dominantly inherited sensory neuropathyC2875301
- Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndromeC3854373
- MORVAN DISC3854373
- MORVAN DISEASEC3854373
- Morvan DiseaseC3854373
- Morvan DiseasesC3854373
- Morvan diseaseC3854373
- Morvan fibrillary choreaC3854373
- Morvan syndromeC3854373
- Morvan syndrome (disorder)C3854373
- Morvan's DiseaseC3854373
- Morvan's DiseasesC3854373
- Morvan's diseaseC3854373
- Morvans DiseaseC3854373
- morvan diseaseC3854373
- morvan's diseaseC3854373
- Nelaton's syndromeC2875302
- Other hereditary and idiopathic neuropathiesC0477392
- Recessively inherited sensory neuropathyC2875303
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: 702423009, 44169009, 1259063005, 702439002, 33994004, 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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.