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 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
- 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
Frequently Asked Questions
What is ICD-10 code G60.9?
ICD-10-CM code G60.9 represents "Hereditary and idiopathic neuropathy, unspecified". It 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.
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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.