G60.0
BillableHereditary motor and sensory neuropathy
Hereditary motor and sensory neuropathy
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
- 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
- Charcot-Marie-Tooth disease, type IC4183003
- Sensory polyneuropathy13694005
- Hypertrophic interstitial neuropathy18708008
- Charcot-Marie-Tooth disease, type IA40632002
- Charcot-Marie-Tooth disease, type IB42986003
- Hereditary ataxia-muscular atrophy syndrome45853006
- Roussy-Levy syndrome45853006
- Roussy-Lévy syndrome45853006
- Axonal neuropathy60703000
- Copper metabolism disorder79886009
- Disorder of copper metabolism79886009
- Motor polyneuropathy85423005
- Charcot-Marie-Tooth disease type 3111499002
- Dejerine-Sottas disease111499002
- Déjérine-Sottas disease111499002
- HMSN III111499002
- HSMN III111499002
- Hereditary hypertrophic neuropathy111499002
- Hereditary motor and sensory neuropathy type III111499002
- Hereditary motor and sensory neuropathy, type III111499002
- Hereditary sensory-motor neuropathy, type III111499002
- Hypertrophic demyelinative neuropathy of infancy111499002
- Hypertrophic hereditary neuropathy111499002
- Progressive hypertrophic interstitial neuropathy111499002
- HMSN VI128203003
- Hereditary motor and sensory neuropathy type VI128203003
- Hereditary motor and sensory neuropathy with optic atrophy128203003
- Hereditary motor-sensory neuropathy with optic atrophy128203003
- Hereditary motor-sensory neuropathy, type VI128203003
- Hereditary sensory and motor neuropathy, type VI128203003
- HMSN VII128204009
- HSMN VII128204009
- Hereditary motor and sensory neuropathy type VII128204009
- Hereditary motor and sensory neuropathy with retinitis pigmentosa128204009
- Hereditary motor and sensory neuropathy, type VII128204009
- Hereditary motor-sensory neuropathy with retinitis pigmentosa128204009
- Hereditary sensory-motor neuropathy, type VII128204009
- Peripheral axonal neuropathy128208007
- ALF - Acute liver failure197270009
- Acute hepatic failure197270009
- Acute liver failure197270009
- Paralysis of glottis226080004
- Distal spinal muscular atrophy230247001
- X-linked Charcot-Marie-Tooth disease230552007
- X-linked hereditary motor and sensory neuropathy230552007
- Hereditary liability to pressure palsies230558006
- Tomaculous neuropathy230558006
- Hereditary hypertrophic neuropathy with paraproteinaemia230559003
- Hereditary hypertrophic neuropathy with paraproteinemia230559003
- Congenital polyneuropathy230560008
- Paralysis of vocal cords302912005
- VCP - Vocal cord palsy302912005
- Vocal cord palsy302912005
- Vocal cord paralysis302912005
- Vocal fold palsy302912005
- Acrodystrophic neuropathy397734008
- Dominant hereditary sensory neuropathy, type I397734008
- Hereditary sensory and autonomic neuropathy type I397734008
- Hereditary sensory and autonomic neuropathy, type I397734008
- Charcot Marie Tooth disease, type 1398040009
- Charcot-Marie-Tooth disease of demyelinating type398040009
- Charcot-Marie-Tooth disease, type I398040009
- HSMN, type I398040009
- Hereditary motor and sensory neuropathy type I398040009
- Hereditary sensory-motor neuropathy, type I398040009
- Inherited dominant hypertrophic neuropathy398040009
- Peroneal muscular atrophy of demyelinating type398040009
- CMT - Charcot-Marie-Tooth disease398100001
- HMSN - hereditary motor and sensory neuropathy398100001
- HSMN - hereditary sensory and motor neuropathy398100001
- Hereditary motor and sensory neuropathy398100001
- Hereditary sensorimotor neuropathy398100001
- Hereditary sensory and motor neuropathy398100001
- Hereditary sensory-motor neuropathy398100001
- Dominant hereditary sensory neuropathy, type II398148000
- Hereditary sensory and autonomic neuropathy type II398148000
- Hereditary sensory and autonomic neuropathy, type II398148000
- Painless whitlow disease398148000
- Charcot Marie Tooth disease, type 2398187000
- Charcot-Marie-Tooth disease, type II398187000
- Hereditary motor and sensory neuropathy type II398187000
- Inherited neuronal peroneal muscular atrophy398187000
- Peroneal muscular atrophy of neuronal type398187000
- Hereditary thermosensitive neuropathy715645004
- Hereditary motor and sensory neuropathy Okinawa type715665006
- Hereditary motor and sensory neuropathy proximal type715665006
- Charcot-Marie-Tooth disease and deafness715666007
- Charcot-Marie-Tooth disease type 1E715666007
- Charcot-Marie-Tooth disease type IE715666007
- Autosomal recessive demyelinating Charcot-Marie-Tooth715795005
- Charcot-Marie-Tooth disease type 4715795005
- Charcot-Marie-Tooth disease type 4A715796006
- Charcot-Marie-Tooth disease type 4C715797002
- Charcot-Marie-Tooth disease type 4D715798007
- Hereditary motor and sensory neuropathy Lom type715798007
- Charcot-Marie-Tooth disease type 4G715799004
- Hereditary motor and sensory neuropathy Russe type715799004
- Charcot-Marie-Tooth disease type 4B2715800000
- Charcot-Marie-Tooth disease type 4F715801001
- Charcot-Marie-Tooth disease type 4H715802008
- Charcot-Marie-Tooth disease type 4B1715803003
- Autosomal dominant Charcot-Marie-Tooth disease type 2B717008005
- Autosomal dominant Charcot-Marie-Tooth disease type 2C717010007
- Autosomal dominant Charcot-Marie-Tooth disease type 2D717011006
- Autosomal dominant Charcot-Marie-Tooth disease type 2E717012004
- Autosomal dominant Charcot-Marie-Tooth disease type 2I717013009
- Autosomal dominant Charcot-Marie-Tooth disease type 2J717014003
- Autosomal dominant Charcot-Marie-Tooth disease type 2A1717016001
- HSAN1B - hereditary sensory and autonomic neuropathy type 1B717825008
- Hereditary sensory and autonomic neuropathy type 1 with cough and gastroesophageal reflux717825008
- Hereditary sensory and autonomic neuropathy type 1 with cough and gastrooesophageal reflux717825008
- Hereditary sensory and autonomic neuropathy type 1B717825008
- HSAN (hereditary sensory and autonomic neuropathy) with deafness and global delay717826009
- Hereditary sensory and autonomic neuropathy with deafness and global delay717826009
- Autosomal dominant Charcot-Marie-Tooth disease type 2F719510006
- Autosomal dominant Charcot-Marie-Tooth disease type 2K719512003
- Autosomal dominant Charcot-Marie-Tooth disease type 2L719513008
- Autosomal dominant Charcot-Marie-Tooth disease type 2M719514002
- Autosomal dominant Charcot-Marie-Tooth disease type 2N719515001
- Charcot-Marie-Tooth disease type 1D719979008
- Charcot-Marie-Tooth disease type ID719979008
- Charcot-Marie-Tooth disease type 1F719980006
- Charcot-Marie-Tooth disease type IF719980006
- Autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2719981005
- Charcot-Marie-Tooth disease type 2B2719981005
- Axonal Charcot-Marie-Tooth disease with pyramidal involvement720637005
- Charcot-Marie-Tooth disease type 2H720637005
- Charcot-Marie-Tooth disease type 4J720638000
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type E722294004
- Charcot-Marie-Tooth disease with nephropathy syndrome722294004
- Autosomal recessive Charcot-Marie-Tooth disease with hoarseness725047007
- Autosomal recessive axonal Charcot-Marie-Tooth disease type 2K725047007
- Autosomal recessive Charcot-Marie-Tooth disease type 2B1725048002
- Charcot-Marie-Tooth disease type 2B1725048002
- Autosomal recessive congenital hypomyelinating neuropathy763135001
- Charcot-Marie-Tooth disease type 4E763135001
- Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome763136000
- Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibers763136000
- Hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibres763136000
- Charcot-Marie-Tooth disease type 4B3763345008
- Charcot-Marie-Tooth disease with focally folded myelin763345008
- X-linked Charcot-Marie-Tooth disease type 6763347000
- Cowchock syndrome763400005
- X-linked Charcot-Marie-Tooth disease type 4763400005
- X-linked Charcot-Marie-Tooth disease type 1763455008
- X-linked Charcot-Marie-Tooth disease type 2763457000
- X-linked Charcot-Marie-Tooth disease type 3763458005
- X-linked Charcot-Marie-Tooth disease type 5763460007
- Microcephalus, complex motor and sensory axonal neuropathy syndrome763798008
- Microcephaly, complex motor and sensory axonal neuropathy syndrome763798008
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation764730007
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation764730007
- Autosomal dominant Charcot-Marie-Tooth disease type 2A2764850002
- Autosomal dominant slowed nerve conduction velocity764854006
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS (methionyl-tRNA synthetase) mutation765046002
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS mutation765046002
- Autosomal dominant Charcot-Marie-Tooth disease type 2U765046002
- Charcot-Marie-Tooth disease type 4K765047006
- SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4765047006
- SURF1-related Charcot-Marie-Tooth disease type 4765047006
- SURF1-related severe demyelinating Charcot-Marie-Tooth disease765047006
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type A765744006
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type B765745007
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type C765746008
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type D765747004
- Autosomal recessive Charcot-Marie-Tooth disease Ouvrier type766977007
- Severe early-onset axonal neuropathy due to MFN2 (mitofusin 2) deficiency766977007
- Severe early-onset axonal neuropathy due to MFN2 deficiency766977007
- Severe early-onset axonal neuropathy due to mitofusin 2 deficiency766977007
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type F770759001
- Distal hereditary motor neuropathy type 7771081007
- Distal spinal muscular atrophy with vocal cord paralysis771081007
- Autosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophy771144005
- Autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy771144005
- Hereditary motor and sensory neuropathy with acrodystrophy771144005
- Autosomal recessive Charcot-Marie-Tooth disease type 2B5771307003
- Charcot-Marie-Tooth disease type 2B5771307003
- Severe early-onset axonal neuropathy due to NEFL (neurofilament light) deficiency771307003
- Severe early-onset axonal neuropathy due to NEFL deficiency771307003
- Severe early-onset axonal neuropathy due to light neurofilament subunit deficiency771307003
- Autosomal recessive distal spinal muscular atrophy type 5771475006
- Young adult-onset distal hereditary motor neuropathy771475006
- Autosomal recessive intermediate Charcot-Marie-Tooth disease type A773308001
- RI-CMT (recessive intermediate Charcot-Marie-Tooth) type A773308001
- Autosomal recessive intermediate Charcot-Marie-Tooth disease type B773330000
- RI-CMT (recessive intermediate Charcot-Marie-Tooth) type B773330000
- Autosomal dominant Charcot-Marie-Tooth disease type 2Q773393001
- Autosomal recessive intermediate Charcot-Marie-Tooth disease type C773414009
- RI-CMT (recessive intermediate Charcot-Marie-Tooth) type C773414009
- Charcot-Marie-Tooth disease type 2R774147002
- Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain778003000
- Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons782742006
- Autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons782742006
- CMT2P - Charcot-Marie-Tooth disease type 2P782826009
- Charcot-Marie-Tooth disease type 2P782826009
- Autosomal dominant Charcot-Marie-Tooth disease type 2O782829002
- Hereditary sensorimotor neuropathy with hyperelastic skin782881002
- 46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome783091003
- Hereditary sensory autonomic neuropathy type IIA860809000
- Hereditary sensory autonomic neuropathy type IIB860810005
- Hereditary sensory autonomic neuropathy type ID860811009
- Hereditary sensory autonomic neuropathy type IE860812002
- Hereditary sensory autonomic neuropathy type IA860813007
- Hereditary sensory autonomic neuropathy type IC860814001
- Amyotrophy of muscle of lower leg1119440005
- Atrophy of muscle of lower leg1119440005
- Atrophy of peroneal muscle1142324004
- Autosomal dominant Charcot-Marie-Tooth disease type 21156835005
- Autosomal dominant distal hereditary motor neuropathy1156837002
- X-linked distal hereditary motor neuropathy1156840002
- Autosomal recessive distal hereditary motor neuropathy1156850001
- Autosomal recessive Charcot-Marie-Tooth disease type 21156852009
- MME-related autosomal dominant Charcot Marie Tooth disease type 21172585006
- MME-related autosomal dominant hereditary motor and sensory neuropathy type 21172585006
- Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 21172585006
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS (histidyl-tRNA synthetase 1) mutation1172634009
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation1172634009
- Autosomal dominant Charcot-Marie-Tooth disease type 2W1172634009
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation1172684002
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to diacylglycerol O-acyltransferase 2 mutation1172684002
- PMP2-related Charcot-Marie-Tooth disease type 11177165005
- PMP2-related Charcot-Marie-Tooth neuropathy type 11177165005
- PMP2-related hereditary motor and sensory neuropathy type 11177165005
- Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 11177165005
- Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome1179294000
- Autosomal recessive axonal Charcot-Marie-Tooth disease type 2T1187128001
- Charcot-Marie-Tooth disease type 2T1187128001
- Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 (SPG11 vesicle trafficking associated, spatacsin) mutation1187563003
- Autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation1187563003
- Autosomal recessive Charcot-Marie-Tooth disease type 2X1187563003
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 (MORC family CW-type zinc finger 2) mutation1187564009
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 mutation1187564009
- Autosomal dominant Charcot-Marie-Tooth disease type 2Z1187564009
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP (valosin containing protein) mutation1187565005
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation1187565005
- Autosomal dominant Charcot-Marie-Tooth disease type 2Y1187565005
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation1187566006
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation1187566006
- Autosomal recessive intermediate Charcot-Marie-Tooth disease type D1187567002
- Charcot-Marie-Tooth disease type 2S1187617004
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU (N-acetyl-alpha-glucosaminidase) mutation1187618009
- Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation1187618009
- Autosomal dominant Charcot-Marie-Tooth disease type 2V1187618009
- Hereditary adult onset painful axonal polyneuropathy1187618009
- Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect1187619001
- ATP1A1 (ATPase Na+/K+ transporting subunit alpha 1) related autosomal dominant Charcot-Marie-Tooth disease type 21187620007
- ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 21187620007
- Autosomal dominant Charcot-Marie-Tooth disease type 2DD1187620007
- DNAJB2-related Charcot-Marie-Tooth disease type 21187621006
- DnaJ heat shock protein family (Hsp40) member B2-related Charcot-Marie-Tooth disease type 21187621006
- Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome1187643003
- Autosomal recessive spinocerebellar ataxia type 211187643003
- Distal hereditary motor neuropathy type 51197152005
- Distal hereditary motor neuropathy type V1197152005
- Distal spinal muscular atrophy type 51197152005
- dHMN5 - distal hereditary motor neuropathy type 51197152005
- Palmoplantar keratoderma, Charcot-Marie-Tooth syndrome1222646006
- Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome1222646006
- Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy1222704008
- Congenital axonal neuropathy with encephalopathy1237626001
- ANOAC (axonal neuropathy, optic atrophy, cognitive deficit) syndrome1260129000
- Axonal neuropathy, optic atrophy, cognitive deficit syndrome1260129000
- Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome1260129000
- Charcot-Marie-Tooth Neuropathy Type 467661000119100
UMLS
- Areflexic Dystasia, HereditaryC0205713
- Areflexic Dystasias, HereditaryC0205713
- Dystasia, Hereditary AreflexicC0205713
- Dystasias, Hereditary AreflexicC0205713
- Hereditary Areflexic DystasiaC0205713
- Hereditary Areflexic DystasiasC0205713
- Hereditary areflexic dystasiaC0205713
- Hereditary ataxia-muscular atrophy syndromeC0205713
- ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIAC0205713
- ROUSSY-LEVY SYNDROMEC0205713
- Roussy Levy DiseaseC0205713
- Roussy Levy Hereditary Areflexic DystasiaC0205713
- Roussy Levy SyndromeC0205713
- Roussy Levy syndromeC0205713
- Roussy-Levy DiseaseC0205713
- Roussy-Levy Hereditary Areflexic DystasiaC0205713
- Roussy-Levy SyndromeC0205713
- Roussy-Levy syndromeC0205713
- Roussy-Lévy syndromeC0205713
- Roussy-Lévy syndrome (disorder)C0205713
- Syndrome, Roussy-LevyC0205713
- hereditary areflexic dystasiaC0205713
- levy-roussy syndromeC0205713
- roussy-levy syndromeC0205713
- Atrophies, Peroneal MuscularC0007959
- Atrophy, Muscular, PeronealC0007959
- Atrophy, Peroneal MuscularC0007959
- CHARCOT MARIE DISC0007959
- CHARCOT MARIE TOOTH DISC0007959
- CMTC0007959
- Charcot Marie DiseaseC0007959
- Charcot Marie Tooth DiseaseC0007959
- Charcot Marie Tooth Hereditary NeuropathyC0007959
- Charcot Marie Tooth SyndromeC0007959
- Charcot Marie Tooth diseaseC0007959
- Charcot Marie Tooth muscular atrophyC0007959
- Charcot-Marie DiseaseC0007959
- Charcot-Marie-Tooth DiseaseC0007959
- Charcot-Marie-Tooth Hereditary NeuropathyC0007959
- Charcot-Marie-Tooth SyndromeC0007959
- Charcot-Marie-Tooth diseaseC0007959
- Charcot-Marie-Tooth hereditary neuropathyC0007959
- Charcot-Marie-Tooth syndromeC0007959
- HMSNC0007959
- Hereditary Neuropathy, Charcot-Marie-ToothC0007959
- Muscular Atrophies, PeronealC0007959
- Muscular Atrophy, PeronealC0007959
- PERONEAL MUSCULAR ATROPHYC0007959
- PMAC0007959
- Peroneal Muscular AtrophiesC0007959
- Peroneal Muscular AtrophyC0007959
- Peroneal muscular atrophyC0007959
- Syndrome, Charcot-Marie-ToothC0007959
- charcot marie tooth diseaseC0007959
- charcot marie tooth syndromeC0007959
- charcot-marie-tooth diseaseC0007959
- charcot-marie-tooth syndromeC0007959
- peroneal muscular atrophyC0007959
- CHARCOT-MARIE-TOOTH DISEASE, TYPE 3C0011195
- CMT3C0011195
- CMT4fC0011195
- Charcot Marie Tooth Disease, Type 3C0011195
- Charcot-Marie-Tooth Disease, Demyelinating, Type 4fC0011195
- Charcot-Marie-Tooth Disease, Type 3C0011195
- Charcot-Marie-Tooth disease type 3C0011195
- DEJERINE SOTTAS DISC0011195
- DEJERINE-SOTTAS NEUROPATHYC0011195
- DEJERINE-SOTTAS SYNDROMEC0011195
- DSNC0011195
- DSSC0011195
- Dejerine Sottas DiseaseC0011195
- Dejerine Sottas NeuropathyC0011195
- Dejerine Sottas SyndromeC0011195
- Dejerine Sottas diseaseC0011195
- Dejerine-Sottas DiseaseC0011195
- Dejerine-Sottas Hypertrophic NeuropathyC0011195
- Dejerine-Sottas NeuropathyC0011195
- Dejerine-Sottas SyndromeC0011195
- Dejerine-Sottas diseaseC0011195
- Disease, Dejerine-SottasC0011195
- Déjérine-Sottas diseaseC0011195
- Déjérine-Sottas disease (disorder)C0011195
- HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE IIIC0011195
- HEREDITARY TYPE III MOTOR SENSORY NEUROPATHYC0011195
- HMSN IIIC0011195
- HMSN Type IIIC0011195
- HMSN Type IIIsC0011195
- HMSN3C0011195
- HSMN IIIC0011195
- HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTASC0011195
- Hereditary Motor and Sensory Neuropathy 3C0011195
- Hereditary Motor and Sensory Neuropathy Type IIIC0011195
- Hereditary hypertrophic neuropathyC0011195
- Hereditary motor and sensory neuropathy type IIIC0011195
- Hereditary motor and sensory neuropathy, type IIIC0011195
- Hereditary sensory-motor neuropathy, type IIIC0011195
- Hereditary, Type III, Motor and Sensory NeuropathyC0011195
- Hypertrophic Neuropathy of Dejerine SottasC0011195
- Hypertrophic Neuropathy of Dejerine-SottasC0011195
- Hypertrophic demyelinative neuropathy of infancyC0011195
- Hypertrophic hereditary neuropathyC0011195
- Neuropathy, Dejerine-SottasC0011195
- Progressive hypertrophic interstitial neuropathyC0011195
- Syndrome, Dejerine-SottasC0011195
- dejerine sottas diseaseC0011195
- dejerine-sottas diseaseC0011195
- dejerines diseases sottasC0011195
- hmsn iiiC0011195
- CMT - Charcot-Marie-Tooth diseaseC0027888
- HEREDITARY MOTOR SENSORY NEUROPATHIESC0027888
- HMSN - hereditary motor and sensory neuropathyC0027888
- HSMN - hereditary sensory and motor neuropathyC0027888
- Herditary Sensory and Motor NeuropathyC0027888
- Hereditary Motor and Sensory NeuropathiesC0027888
- Hereditary Motor and Sensory NeuropathyC0027888
- Hereditary Sensorimotor NeuropathyC0027888
- Hereditary Sensory and Motor NeuropathyC0027888
- Hereditary motor and sensory neuropathyC0027888
- Hereditary motor and sensory neuropathy (disorder)C0027888
- Hereditary sensorimotor neuropathyC0027888
- Hereditary sensory and motor neuropathyC0027888
- Hereditary sensory-motor neuropathyC0027888
- NEUROPATHIES HEREDITARY MOTOR SENSORYC0027888
- Neuropathic muscular atrophyC0027888
- Neuropathies, Hereditary Motor and SensoryC0027888
- hereditary motor and sensory neuropathies (HMSN)C0027888
- hereditary motor and sensory neuropathyC0027888
- hmsnC0027888
- neuropathic muscular atrophyC0027888
- Hereditary motor and sensory neuropathy, types I-IVC1408182
- Hypertrophic neuropathy of infancyC1408174
- Peroneal muscular atrophy (axonal type) (hypertrophic type)C2875300
Frequently Asked Questions
What is ICD-10 code G60.0?
ICD-10-CM code G60.0 represents "Hereditary motor and sensory neuropathy". It 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: 128203003, 128204009, 783091003, 197270009, 1260129000, 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.
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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.