AutoICD API

G60.0

Billable

Hereditary motor and sensory neuropathy

Hereditary motor and sensory neuropathy

Status

Billable / Specific

Block

G60-G65

Parent Code

G60

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Charcot-Marie-Tooth disease
  • Déjérine-Sottas disease
  • Hereditary motor and sensory neuropathy, types I-IV
  • Hypertrophic neuropathy of infancy
  • Peroneal muscular atrophy (axonal type) (hypertrophic type)
  • Roussy-Levy syndrome

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)
G60.1

Refsum's disease

BillableG60.2

Neuropathy in association with hereditary ataxia

BillableG60.3

Idiopathic progressive neuropathy

BillableG60.8

Other hereditary and idiopathic neuropathies

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

8C20.ZHereditary motor and sensory neuropathy, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(736)

SNOMED CT

UMLS

Clinical Terms

  • Charcot-Marie-Tooth disease type 2R
  • X-linked Charcot-Marie-Tooth disease type 1
  • hereditary motor and sensory neuropathies (HMSN)
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
  • Peripheral axonal neuropathy
  • HEREDITARY MOTOR SENSORY NEUROPATHIES
  • Vocal cord palsy
  • Neuropathic muscular atrophy
  • Charcot-Marie-Tooth disease type 4D
  • Autosomal recessive Charcot-Marie-Tooth disease type 2X
  • Charcot-Marie-Tooth disease and deafness
  • Charcot-Marie-Tooth disease, type IA
  • Hereditary Sensory and Motor Neuropathy
  • CMT - Charcot-Marie-Tooth disease
  • Autosomal dominant Charcot-Marie-Tooth disease type 2W
  • DEJERINE-SOTTAS SYNDROME
  • Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
  • Herditary Sensory and Motor Neuropathy
  • Roussy-Levy syndrome
  • Hereditary Areflexic Dystasia
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
  • Hereditary motor and sensory neuropathy with retinitis pigmentosa
  • dejerines diseases sottas
  • Hereditary motor and sensory neuropathy (disorder)
  • Hereditary sensory autonomic neuropathy type IC
  • HSAN (hereditary sensory and autonomic neuropathy) with deafness and global delay
  • Hereditary hypertrophic neuropathy with paraproteinemia
  • Hereditary sensory and autonomic neuropathy type 1 with cough and gastroesophageal reflux
  • Autosomal dominant Charcot-Marie-Tooth disease type 2DD
  • Charcot-Marie-Tooth disease type 2P
  • Hereditary sensory and autonomic neuropathy type I
  • dHMN5 - distal hereditary motor neuropathy type 5
  • Autosomal recessive axonal Charcot-Marie-Tooth disease type 2K
  • VCP - Vocal cord palsy
  • Areflexic Dystasias, Hereditary
  • Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1
  • Autosomal dominant Charcot-Marie-Tooth disease type 2O
  • Severe early-onset axonal neuropathy due to MFN2 (mitofusin 2) deficiency
  • Autosomal dominant Charcot-Marie-Tooth disease type 2B
  • Hereditary sensory and autonomic neuropathy type II
  • CMT4f
  • Charcot-Marie-Tooth disease type 3
  • Atrophies, Peroneal Muscular
  • Dejerine-Sottas Neuropathy
  • PERONEAL MUSCULAR ATROPHY
  • Autosomal dominant distal hereditary motor neuropathy
  • Hereditary motor and sensory neuropathy, type III
  • HMSN3
  • Autosomal dominant Charcot-Marie-Tooth disease type 2L
  • Roussy-Lévy syndrome (disorder)
  • Charcot-Marie-Tooth disease type IE
  • charcot marie tooth syndrome
  • Hereditary hypertrophic neuropathy with paraproteinaemia
  • HMSN VII
  • PMP2-related hereditary motor and sensory neuropathy type 1
  • Autosomal dominant Charcot-Marie-Tooth disease type 2U
  • Autosomal recessive demyelinating Charcot-Marie-Tooth
  • Severe early-onset axonal neuropathy due to MFN2 deficiency
  • Hereditary sensory and autonomic neuropathy type 1B
  • Dominant hereditary sensory neuropathy, type II
  • Hereditary motor-sensory neuropathy with optic atrophy
  • Hereditary sensory and autonomic neuropathy, type I
  • Hypertrophic neuropathy of infancy
  • Charcot-Marie-Tooth disease type 4B3
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation
  • Hereditary motor and sensory neuropathy type I
  • Progressive hypertrophic interstitial neuropathy
  • Charcot-Marie-Tooth disease type 4A
  • Motor polyneuropathy
  • RI-CMT (recessive intermediate Charcot-Marie-Tooth) type B
  • Hereditary sensory and autonomic neuropathy with deafness and global delay
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
  • Hereditary motor and sensory neuropathy Russe type
  • Charcot-Marie-Tooth disease type 2B1
  • Autosomal dominant Charcot-Marie-Tooth disease type 2D
  • Hereditary sensory autonomic neuropathy type IA
  • Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibers
  • Sensory polyneuropathy
  • Charcot-Marie-Tooth Disease
  • Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2
  • Hereditary sensorimotor neuropathy with hyperelastic skin
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
  • Hereditary motor and sensory neuropathy proximal type
  • Charcot-Marie-Tooth disease type IF
  • Charcot-Marie-Tooth disease, type IC
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
  • Hereditary sensory-motor neuropathy, type VII
  • Young adult-onset distal hereditary motor neuropathy
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation
  • Muscular Atrophies, Peroneal
  • HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE III
  • 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome
  • Autosomal recessive Charcot-Marie-Tooth disease type 2B5
  • Charcot-Marie-Tooth disease type 4K
  • Autosomal dominant Charcot-Marie-Tooth disease type 2V
  • Muscular Atrophy, Peroneal
  • Charcot Marie Disease
  • X-linked distal hereditary motor neuropathy
  • Charcot-Marie Disease
  • Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome
  • hmsn
  • HEREDITARY TYPE III MOTOR SENSORY NEUROPATHY
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU (N-acetyl-alpha-glucosaminidase) mutation
  • HMSN Type IIIs
  • CHARCOT-MARIE-TOOTH DISEASE, TYPE 3
  • Autosomal dominant Charcot-Marie-Tooth disease type 2J
  • ALF - Acute liver failure
  • Hereditary sensory-motor neuropathy, type III
  • Axonal neuropathy
  • Autosomal dominant Charcot-Marie-Tooth disease type 2C
  • Charcot-Marie-Tooth disease type 4E
  • Déjérine-Sottas disease
  • CMT3
  • Hereditary Areflexic Dystasias
  • Autosomal recessive distal spinal muscular atrophy type 5
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
  • HMSN - hereditary motor and sensory neuropathy
  • Autosomal dominant Charcot-Marie-Tooth disease type 2F
  • Charcot-Marie-Tooth disease type 1F
  • Charcot-Marie-Tooth disease, type IB
  • MME-related autosomal dominant hereditary motor and sensory neuropathy type 2
  • Distal hereditary motor neuropathy type V
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS mutation
  • Charcot-Marie-Tooth disease type 2T
  • Mixed sensory-motor polyneuropathy
  • X-linked Charcot-Marie-Tooth disease type 3
  • Charcot-Marie-Tooth Hereditary Neuropathy
  • HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS
  • Syndrome, Dejerine-Sottas
  • PMA
  • Autosomal dominant Charcot-Marie-Tooth disease type 2Q
  • Autosomal dominant Charcot-Marie-Tooth disease type 2N
  • Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome
  • Dominant hereditary sensory neuropathy, type I
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 (MORC family CW-type zinc finger 2) mutation
  • Inherited dominant hypertrophic neuropathy
  • Charcot-Marie-Tooth disease type 1D
  • Inherited neuronal peroneal muscular atrophy
  • Autosomal dominant Charcot-Marie-Tooth disease type 2I
  • ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA
  • Charcot-Marie-Tooth disease type 2S
  • Hereditary motor and sensory neuropathy Lom type
  • Peroneal Muscular Atrophies
  • Hereditary motor and sensory neuropathy Okinawa type
  • Hereditary sensory and motor neuropathy, type VI
  • Hereditary motor and sensory neuropathy type VII
  • Dystasia, Hereditary Areflexic
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation
  • Peroneal muscular atrophy (axonal type) (hypertrophic type)
  • Charcot-Marie-Tooth disease type ID
  • RI-CMT (recessive intermediate Charcot-Marie-Tooth) type A
  • Autosomal dominant slowed nerve conduction velocity
  • Charcot-Marie-Tooth syndrome
  • X-linked Charcot-Marie-Tooth disease type 2
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
  • Peroneal muscular atrophy of neuronal type
  • Autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2
  • Hypertrophic hereditary neuropathy
  • Roussy Levy syndrome
  • Syndrome, Roussy-Levy
  • HSMN VII
  • Atrophy of peroneal muscle
  • Dejerine-Sottas Disease
  • ATP1A1 (ATPase Na+/K+ transporting subunit alpha 1) related autosomal dominant Charcot-Marie-Tooth disease type 2
  • Hereditary sensory-motor neuropathy
  • DSS
  • DnaJ heat shock protein family (Hsp40) member B2-related Charcot-Marie-Tooth disease type 2
  • HSAN1B - hereditary sensory and autonomic neuropathy type 1B
  • Distal spinal muscular atrophy with vocal cord paralysis
  • CHARCOT MARIE DIS
  • Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 (SPG11 vesicle trafficking associated, spatacsin) mutation
  • Hereditary liability to pressure palsies
  • DEJERINE SOTTAS DIS
  • Hereditary sensory and autonomic neuropathy, type II
  • Copper metabolism disorder
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
  • Hereditary thermosensitive neuropathy
  • Palmoplantar keratoderma, Charcot-Marie-Tooth syndrome
  • Hereditary sensory autonomic neuropathy type ID
  • Roussy Levy Disease
  • Hypertrophic demyelinative neuropathy of infancy
  • Hereditary Motor and Sensory Neuropathies
  • Axonal neuropathy, optic atrophy, cognitive deficit syndrome
  • Autosomal dominant Charcot-Marie-Tooth disease type 2E
  • Autosomal dominant Charcot-Marie-Tooth disease type 2Y
  • PMP2-related Charcot-Marie-Tooth neuropathy type 1
  • Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
  • Hereditary motor and sensory neuropathy, types I-IV
  • Hypertrophic interstitial neuropathy
  • Hereditary ataxia-muscular atrophy syndrome
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to diacylglycerol O-acyltransferase 2 mutation
  • Atrophy of muscle of lower leg
  • SURF1-related Charcot-Marie-Tooth disease type 4
  • Autosomal recessive spinocerebellar ataxia type 21
  • Hereditary motor and sensory neuropathy, type VII
  • Autosomal dominant Charcot-Marie-Tooth disease type 2
  • Congenital axonal neuropathy with encephalopathy
  • CMT2P - Charcot-Marie-Tooth disease type 2P
  • Atrophy, Peroneal Muscular
  • Charcot-Marie-Tooth disease type 4F
  • Charcot Marie Tooth Disease
  • X-linked Charcot-Marie-Tooth disease
  • Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome
  • Hereditary sensory and autonomic neuropathy type 1 with cough and gastrooesophageal reflux
  • Distal spinal muscular atrophy
  • Paralysis of glottis
  • Congenital polyneuropathy
  • Charcot Marie Tooth disease, type 2
  • Hereditary Sensorimotor Neuropathy
  • Hereditary motor-sensory neuropathy, type VI
  • Syndrome, Charcot-Marie-Tooth
  • PMP2-related Charcot-Marie-Tooth disease type 1
  • Severe early-onset axonal neuropathy due to NEFL (neurofilament light) deficiency
  • Hereditary motor-sensory neuropathy with retinitis pigmentosa
  • Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
  • Autosomal dominant Charcot-Marie-Tooth disease type 2A2
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
  • dejerine sottas disease
  • Autosomal dominant Charcot-Marie-Tooth disease type 2K
  • Acute hepatic failure
  • Autosomal recessive Charcot-Marie-Tooth disease type 2
  • HMSN III
  • CMT
  • Microcephalus, complex motor and sensory axonal neuropathy syndrome
  • Charcot Marie Tooth disease, type 1
  • CHARCOT MARIE TOOTH DIS
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 mutation
  • Acute liver failure
  • Autosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophy
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation
  • Charcot-Marie-Tooth disease with focally folded myelin
  • Autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons
  • Charcot Marie Tooth Hereditary Neuropathy
  • Disorder of copper metabolism
  • HMSN VI
  • Autosomal recessive Charcot-Marie-Tooth disease type 2B1
  • Tomaculous neuropathy
  • Autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation
  • Charcot-Marie-Tooth disease type 4
  • Charcot Marie Tooth muscular atrophy
  • Peroneal muscular atrophy of demyelinating type
  • Charcot-Marie-Tooth disease, type II
  • Hereditary sensory autonomic neuropathy type IE
  • RI-CMT (recessive intermediate Charcot-Marie-Tooth) type C
  • Cowchock syndrome
  • ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2
  • NEUROPATHIES HEREDITARY MOTOR SENSORY
  • DNAJB2-related Charcot-Marie-Tooth disease type 2
  • Hereditary sensory-motor neuropathy, type I
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
  • Dejerine-Sottas Hypertrophic Neuropathy
  • Autosomal recessive distal hereditary motor neuropathy
  • Déjérine-Sottas disease (disorder)
  • HSMN III
  • Charcot-Marie-Tooth disease type 4C
  • Charcot-Marie-Tooth disease type 4G
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
  • Hereditary sensory autonomic neuropathy type IIB
  • Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy
  • Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome
  • Severe early-onset axonal neuropathy due to NEFL deficiency
  • Charcot-Marie-Tooth disease with nephropathy syndrome
  • Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibres
  • Axonal Charcot-Marie-Tooth disease with pyramidal involvement
  • Charcot-Marie-Tooth disease type 4J
  • X-linked hereditary motor and sensory neuropathy
  • Roussy-Levy Disease
  • SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4
  • Hereditary motor and sensory neuropathy with acrodystrophy
  • Amyotrophy of muscle of lower leg
  • Hereditary sensory autonomic neuropathy type IIA
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation
  • ANOAC (axonal neuropathy, optic atrophy, cognitive deficit) syndrome
  • SURF1-related severe demyelinating Charcot-Marie-Tooth disease
  • Charcot-Marie-Tooth disease type 4B2
  • Dejerine Sottas Syndrome
  • Vocal cord paralysis
  • Charcot-Marie-Tooth disease type 2B5
  • Charcot-Marie-Tooth disease type 4H
  • Charcot-Marie-Tooth Neuropathy Type 4
  • Painless whitlow disease
  • DSN
  • Neuropathies, Hereditary Motor and Sensory
  • Autosomal dominant Charcot-Marie-Tooth disease type 2Z
  • X-linked Charcot-Marie-Tooth disease type 5
  • Roussy-Lévy syndrome
  • Hereditary hypertrophic neuropathy
  • levy-roussy syndrome
  • Charcot-Marie-Tooth disease type 1E
  • Disease, Dejerine-Sottas
  • Charcot-Marie-Tooth disease of demyelinating type
  • Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
  • Distal hereditary motor neuropathy type 5
  • Areflexic Dystasia, Hereditary
  • HSMN, type I
  • Autosomal dominant Charcot-Marie-Tooth disease type 2M
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS (histidyl-tRNA synthetase 1) mutation
  • Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
  • HSMN - hereditary sensory and motor neuropathy
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS (methionyl-tRNA synthetase) mutation
  • Dejerine Sottas Neuropathy
  • Hereditary Motor and Sensory Neuropathy 3
  • Hereditary, Type III, Motor and Sensory Neuropathy
  • Hereditary motor and sensory neuropathy type II
  • Roussy Levy Hereditary Areflexic Dystasia
  • Charcot Marie Tooth Disease, Type 3
  • Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
  • Distal spinal muscular atrophy type 5
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
  • Paralysis of vocal cords
  • Neuropathy, Dejerine-Sottas
  • Charcot-Marie-Tooth disease type 4B1
  • Distal hereditary motor neuropathy type 7
  • Autosomal recessive axonal Charcot-Marie-Tooth disease type 2T
  • MME-related autosomal dominant Charcot Marie Tooth disease type 2
  • Hereditary motor and sensory neuropathy with optic atrophy
  • Charcot-Marie-Tooth disease type 2H
  • X-linked Charcot-Marie-Tooth disease type 4
  • Microcephaly, complex motor and sensory axonal neuropathy syndrome
  • Hereditary motor and sensory neuropathy type VI
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP (valosin containing protein) mutation
  • Hereditary Neuropathy, Charcot-Marie-Tooth
  • Hereditary adult onset painful axonal polyneuropathy
  • X-linked Charcot-Marie-Tooth disease type 6
  • HMSN Type III
  • Acrodystrophic neuropathy
  • Atrophy, Muscular, Peroneal
  • Charcot-Marie-Tooth disease type 2B2
  • Charcot-Marie-Tooth disease, type I
  • Dystasias, Hereditary Areflexic
  • Severe early-onset axonal neuropathy due to light neurofilament subunit deficiency
  • Autosomal recessive congenital hypomyelinating neuropathy
  • Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation
  • Autosomal recessive Charcot-Marie-Tooth disease Ouvrier type
  • Hypertrophic Neuropathy of Dejerine Sottas
  • Autosomal dominant Charcot-Marie-Tooth disease type 2A1
  • Vocal fold palsy
Frequently Asked Questions
What is the ICD-10 code for hereditary motor and sensory neuropathy?

The ICD-10-CM code for hereditary motor and sensory neuropathy is G60.0. The full clinical description is "Hereditary motor and sensory neuropathy". G60.0 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code G60.0 mean?

ICD-10-CM code G60.0 represents “Hereditary motor and sensory neuropathy”. 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 G60.0 a billable code?

Yes, G60.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is G60.0 in?

G60.0 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).

What codes cannot be used with G60.0?

G60.0 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 G60.0 map to?

G60.0 maps to 133 SNOMED CT concepts: 783091003, 197270009, 1260129000, 1187620007, 397734008, and 128 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for G60.0?

G60.0 is linked to 7 UMLS Concept Unique Identifiers: C0205713, C0007959, C0011195, C0027888, C1408182, and 2 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does G60.0 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hereditary motor and sensory neuropathy 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 G60.0?

G60.0 maps to the ICD-11 code: 8C20.Z (Hereditary motor and sensory neuropathy, unspecified).

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.

Try FreeView API Docs

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.