Diagnosis Code: G60.0

Short Description: Hereditary motor and sensory neuropathy

Long Description: Hereditary motor and sensory neuropathy

The code G60.0 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Polyneuropathies and other disorders of the peripheral nervous system (G60-G65)
    • Hereditary and idiopathic neuropathy (G60)
      • G60.0 Hereditary motor and sensory neuropathy

Code Version: 2022 ICD-10-CM

Synonyms

• 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome
• Acute hepatic failure
• Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome
• Autosomal dominant Charcot-Marie-Tooth disease type 2
• Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation
• Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
• Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
• Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
• Autosomal dominant Charcot-Marie-Tooth disease type 2A1
• Autosomal dominant Charcot-Marie-Tooth disease type 2A2
• Autosomal dominant Charcot-Marie-Tooth disease type 2B
• Autosomal dominant Charcot-Marie-Tooth disease type 2C
• Autosomal dominant Charcot-Marie-Tooth disease type 2D
• Autosomal dominant Charcot-Marie-Tooth disease type 2DD
• Autosomal dominant Charcot-Marie-Tooth disease type 2E
• Autosomal dominant Charcot-Marie-Tooth disease type 2F
• Autosomal dominant Charcot-Marie-Tooth disease type 2G
• Autosomal dominant Charcot-Marie-Tooth disease type 2I
• Autosomal dominant Charcot-Marie-Tooth disease type 2J
• Autosomal dominant Charcot-Marie-Tooth disease type 2K
• Autosomal dominant Charcot-Marie-Tooth disease type 2L
• Autosomal dominant Charcot-Marie-Tooth disease type 2M
• Autosomal dominant Charcot-Marie-Tooth disease type 2N
• Autosomal dominant Charcot-Marie-Tooth disease type 2O
• Autosomal dominant Charcot-Marie-Tooth disease type 2Q
• Autosomal dominant Charcot-Marie-Tooth disease type 2U
• Autosomal dominant Charcot-Marie-Tooth disease type 2V
• Autosomal dominant Charcot-Marie-Tooth disease type 2W
• Autosomal dominant Charcot-Marie-Tooth disease type 2Y
• Autosomal dominant Charcot-Marie-Tooth disease type 2Z
• Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome
• Autosomal dominant distal hereditary motor neuropathy
• Autosomal dominant distal hereditary motor neuropathy
• Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
• Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
• Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
• Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
• Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
• Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
• Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
• Autosomal dominant slowed nerve conduction velocity
• Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
• Autosomal recessive Charcot-Marie-Tooth disease type 2
• Autosomal recessive Charcot-Marie-Tooth disease type 2
• Autosomal recessive Charcot-Marie-Tooth disease type 2X
• Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
• Autosomal recessive distal hereditary motor neuropathy
• Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
• Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
• Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
• Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
• Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy
• Axonal neuropathy
• Axonal neuropathy
• Axonal neuropathy
• Charcot-Marie-Tooth disease type 2B1
• Charcot-Marie-Tooth disease type 2B2
• Charcot-Marie-Tooth disease type 2B5
• Charcot-Marie-Tooth disease type 2H
• Charcot-Marie-Tooth disease type 2P
• Charcot-Marie-Tooth disease type 2R
• Charcot-Marie-Tooth disease type 2S
• Charcot-Marie-Tooth disease type 2T
• Charcot-Marie-Tooth disease type 4
• Charcot-Marie-Tooth disease type 4A
• Charcot-Marie-Tooth disease type 4B1
• Charcot-Marie-Tooth disease type 4B2
• Charcot-Marie-Tooth disease type 4B3
• Charcot-Marie-Tooth disease type 4C
• Charcot-Marie-Tooth disease type 4D
• Charcot-Marie-Tooth disease type 4E
• Charcot-Marie-Tooth disease type 4F
• Charcot-Marie-Tooth disease type 4G
• Charcot-Marie-Tooth disease type 4H
• Charcot-Marie-Tooth disease type 4J
• Charcot-Marie-Tooth disease type ID
• Charcot-Marie-Tooth disease type IE
• Charcot-Marie-Tooth disease type IF
• Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
• Charcot-Marie-Tooth disease, type IA
• Charcot-Marie-Tooth disease, type IB
• Charcot-Marie-Tooth disease, type IC
• Charcot-Marie-Tooth disease, type II
• Charcot-Marie-Tooth Neuropathy Type 4
• Congenital axonal neuropathy with encephalopathy
• Congenital polyneuropathy
• Déjérine-Sottas disease
• Disorder of copper metabolism
• Distal hereditary motor neuropathy type 5
• Distal hereditary motor neuropathy type 7
• Distal spinal muscular atrophy
• DNAJB2-related Charcot-Marie-Tooth disease type 2
• Hereditary hypertrophic neuropathy with paraproteinemia
• Hereditary liability to pressure palsies
• Hereditary motor and sensory neuropathy
• Hereditary motor and sensory neuropathy Okinawa type
• Hereditary motor and sensory neuropathy with acrodystrophy
• Hereditary motor and sensory neuropathy with optic atrophy
• Hereditary motor and sensory neuropathy with retinitis pigmentosa
• Hereditary sensorimotor neuropathy with hyperelastic skin
• Hereditary sensory and autonomic neuropathy type 1B
• Hereditary sensory and autonomic neuropathy type I
• Hereditary sensory and autonomic neuropathy type II
• Hereditary sensory and autonomic neuropathy with deafness and global delay
• Hereditary sensory autonomic neuropathy type IA
• Hereditary sensory autonomic neuropathy type IC
• Hereditary sensory autonomic neuropathy type ID
• Hereditary sensory autonomic neuropathy type IE
• Hereditary sensory autonomic neuropathy type IIA
• Hereditary sensory autonomic neuropathy type IIB
• Hereditary sensory-motor neuropathy, type I
• Hereditary thermosensitive neuropathy
• Hypertrophic interstitial neuropathy
• Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome
• Microcephalus, complex motor and sensory axonal neuropathy syndrome
• Mixed sensory-motor polyneuropathy
• Mixed sensory-motor polyneuropathy
• MME-related autosomal dominant Charcot Marie Tooth disease type 2
• Motor polyneuropathy
• Motor polyneuropathy
• Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome
• Paralysis of glottis
• Peripheral axonal neuropathy
• PMP2-related Charcot-Marie-Tooth disease type 1
• Roussy-Lévy syndrome
• Sensory polyneuropathy
• Sensory polyneuropathy
• Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
• SURF1-related Charcot-Marie-Tooth disease type 4
• Vocal cord paralysis
• X-linked Charcot-Marie-Tooth disease type 1
• X-linked Charcot-Marie-Tooth disease type 2
• X-linked Charcot-Marie-Tooth disease type 3
• X-linked Charcot-Marie-Tooth disease type 4
• X-linked Charcot-Marie-Tooth disease type 5
• X-linked Charcot-Marie-Tooth disease type 6
• X-linked distal hereditary motor neuropathy
• X-linked hereditary motor and sensory neuropathy
• Young adult-onset distal hereditary motor neuropathy

References to Index of Diseases and Injuries

The code G60.0 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • 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

Crosswalk Information

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This page was last updated on: 10/1/2023

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