G60.9
BillableHereditary and idiopathic neuropathy, unspecified
Hereditary and idiopathic neuropathy, unspecified
Coding Notes
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 periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(5)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(68)
SNOMED CT
- Idiopathic peripheral neuropathy22722001
- Hereditary peripheral neuropathy65017003
- Micromelia74370006
- Micromelic dwarf74370006
- Micromelus74370006
- Nanomelia74370006
- Optic nerve finding106152006
- Second cranial nerve finding106152006
- Chronic neuropathy with no known cause or association230655004
- Idiopathic chronic neuropathy230655004
- Chronic deafness232325008
- POF - Premature ovarian failure237788002
- Premature ovarian failure237788002
- CCFDN - congenital cataracts, facial dysmorphism and neuropathy702433001
- Congenital cataracts, facial dysmorphism and neuropathy702433001
- CEDNIK (cerebral dysgenesis, neuropathy, ichthyosis, keratoderma) syndrome722385008
- CEDNIK syndrome722385008
- Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome722385008
- Neuropathy with hearing impairment723497003
- Peripheral neuropathy with sensorineural hearing impairment syndrome723497003
- SPOAN (spastic paraplegia, optic atrophy, neuropathy) syndrome725139005
- Spastic paraplegia, optic atrophy, neuropathy syndrome725139005
- Lundberg syndrome770679002
- Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome770679002
- AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- AFG3L2-related spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- Autosomal recessive spastic ataxia type 5771469002
- Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome771469002
- Peripheral neuropathy, myopathy, hoarseness, deafness syndrome782752005
- Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome782752005
- SPOAN and SPOAN-related disorder789674008
- Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder789674008
- Autosomal dominant distal hereditary motor neuropathy1156837002
UMLS
Clinical Terms
- CEDNIK syndrome
- AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
- POF - Premature ovarian failure
- CEDNIK (cerebral dysgenesis, neuropathy, ichthyosis, keratoderma) syndrome
- Micromelia
- Peripheral neuropathy, myopathy, hoarseness, deafness syndrome
- Micromelus
- Autosomal recessive spastic ataxia type 5
- SPOAN and SPOAN-related disorder
- Premature ovarian failure
- SPOAN (spastic paraplegia, optic atrophy, neuropathy) syndrome
- Peripheral neuropathy with sensorineural hearing impairment syndrome
- Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome
- Lundberg syndrome
- Spastic paraplegia, optic atrophy, neuropathy syndrome
- Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome
- Micromelic dwarf
- AFG3L2-related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
- Hereditary peripheral neuropathy
- CCFDN - congenital cataracts, facial dysmorphism and neuropathy
- Chronic deafness
- Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome
- Autosomal dominant distal hereditary motor neuropathy
- Idiopathic peripheral neuropathy
- Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome
- Neuropathy with hearing impairment
- Chronic neuropathy with no known cause or association
- Second cranial nerve finding
- Optic nerve finding
- Nanomelia
- Idiopathic chronic neuropathy
- Congenital cataracts, facial dysmorphism and neuropathy
- Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder
Frequently Asked Questions
What is the ICD-10 code for hereditary and idiopathic neuropathy, unspecified?
The ICD-10-CM code for hereditary and idiopathic neuropathy, unspecified is G60.9. The full clinical description is "Hereditary and idiopathic neuropathy, unspecified". G60.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G60.9 mean?
ICD-10-CM code G60.9 represents “Hereditary and idiopathic neuropathy, unspecified”. 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 G60.9 a billable code?
Yes, G60.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G60.9 in?
G60.9 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G60.9?
G60.9 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 G60.9 map to?
G60.9 maps to 16 SNOMED CT concepts: 771469002, 1156837002, 702433001, 722385008, 232325008, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G60.9?
G60.9 is linked to 1 UMLS Concept Unique Identifier: C0154754. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G60.9 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary and idiopathic neuropathy, unspecified 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 G60.9?
G60.9 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.