| Descriptor English: | Charcot-Marie-Tooth Disease | ||||||
| Descriptor Spanish: |
Enfermedad de Charcot-Marie-Tooth
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| Descriptor Portuguese: | Doença de Charcot-Marie-Tooth | ||||||
| Descriptor French: | Maladie de Charcot-Marie-Tooth | ||||||
| Entry term(s): |
Areflexic Dystasia, Hereditary Areflexic Dystasias, Hereditary Atrophies, Peroneal Muscular Atrophy, Muscular, Peroneal Atrophy, Peroneal Muscular Charcot Marie Disease Charcot Marie Tooth Disease Charcot Marie Tooth Disease, Type 1A Charcot Marie Tooth Disease, Type 1B Charcot Marie Tooth Disease, Type I Charcot Marie Tooth Disease, Type IA Charcot Marie Tooth Disease, Type IB Charcot Marie Tooth Disease, Type II Charcot Marie Tooth Hereditary Neuropathy Charcot Marie Tooth Neuropathy, Type 1A Charcot Marie Tooth Neuropathy, Type 1B Charcot Marie Tooth Syndrome Charcot-Marie Disease Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B Charcot-Marie-Tooth Disease, Demyelinating, Type 1A Charcot-Marie-Tooth Disease, Demyelinating, Type 1B Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy Charcot-Marie-Tooth Disease, Type 1A Charcot-Marie-Tooth Disease, Type 1B Charcot-Marie-Tooth Disease, Type I Charcot-Marie-Tooth Disease, Type IA Charcot-Marie-Tooth Disease, Type IB Charcot-Marie-Tooth Disease, Type II Charcot-Marie-Tooth Hereditary Neuropathy Charcot-Marie-Tooth Neuropathy, Type 1A Charcot-Marie-Tooth Neuropathy, Type 1B Charcot-Marie-Tooth Syndrome Dystasia, Hereditary Areflexic Dystasias, Hereditary Areflexic HMN Distal Type I HMSN 1A HMSN 1B HMSN I HMSN IA HMSN IB HMSN II HMSN Type I HMSN Type II HMSN1A HMSN1B Hereditary Areflexic Dystasia Hereditary Areflexic Dystasias Hereditary Motor And Sensory Neuropathy IB Hereditary Motor and Sensory Neuropathy 1A Hereditary Motor and Sensory Neuropathy 1B Hereditary Motor and Sensory Neuropathy IA Hereditary Motor and Sensory Neuropathy Type II Hereditary Motor and Sensory-Neuropathy Type II Hereditary Motor, and Sensory Neuropathy Type I Hereditary Neuropathy, Charcot-Marie-Tooth Hereditary Type I Motor and Sensory Neuropathy Muscular Atrophies, Peroneal Muscular Atrophy, Peroneal Neuropathy, Type I Hereditary Motor and Sensory Neuropathy, Type II Hereditary Motor and Sensory Peroneal Muscular Atrophies Peroneal Muscular Atrophy Roussy Levy Disease Roussy Levy Hereditary Areflexic Dystasia Roussy Levy Syndrome Roussy-Levy Disease Roussy-Levy Hereditary Areflexic Dystasia Roussy-Levy Syndrome Syndrome, Charcot-Marie-Tooth Syndrome, Roussy-Levy |
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| Tree number(s): |
C10.500.300.200 C10.574.500.495.200 C10.668.829.800.300.200 C16.131.666.300.200 C16.320.400.375.200 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D002607 | ||||||
| Scope note: | A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343) |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2000; see CHARCOT-MARIE DISEASE 1991-1999, see MUSCULAR ATROPHY, SPINAL 1988-1990, see MUSCULAR ATROPHY 1966-1987; for CHARCOT-MARIE-TOOTH DISEASE see CHARCOT-MARIE DISEASE 1991-1999 |
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| History Note: | 2000(1966) |
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| Entry Version: | CHARCOT MARIE TOOTH DIS |
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| Related: |
Myelin P0 Protein
MeSH | ||||||
| DeCS ID: | 24021 | ||||||
| Unique ID: | D002607 | ||||||
| NLM Classification: | WE 550 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1999/11/08 | ||||||
| Revision Date: | 2013/07/08 |
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Charcot-Marie-Tooth Disease
- Preferred
Roussy-Levy Syndrome
- Related but not broader or narrower
Hereditary Type I Motor and Sensory Neuropathy
- Narrower
HMSN Type II
- Narrower
Charcot-Marie-Tooth Disease, Type IA
- Narrower
Charcot-Marie-Tooth Disease, Type IB
- Narrower
| Concept UI |
M0003994 |
| Scope note | A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343) |
| Preferred term | Charcot-Marie-Tooth Disease |
| Entry term(s) |
Atrophies, Peroneal Muscular Atrophy, Muscular, Peroneal Atrophy, Peroneal Muscular Charcot Marie Disease Charcot Marie Tooth Disease Charcot Marie Tooth Hereditary Neuropathy Charcot Marie Tooth Syndrome Charcot-Marie Disease Charcot-Marie-Tooth Hereditary Neuropathy Charcot-Marie-Tooth Syndrome Hereditary Neuropathy, Charcot-Marie-Tooth Muscular Atrophies, Peroneal Muscular Atrophy, Peroneal Peroneal Muscular Atrophies Peroneal Muscular Atrophy Syndrome, Charcot-Marie-Tooth |
| Concept UI |
M0003995 |
| Preferred term | Roussy-Levy Syndrome |
| Entry term(s) |
Areflexic Dystasia, Hereditary Areflexic Dystasias, Hereditary Dystasia, Hereditary Areflexic Dystasias, Hereditary Areflexic Hereditary Areflexic Dystasia Hereditary Areflexic Dystasias Roussy Levy Disease Roussy Levy Hereditary Areflexic Dystasia Roussy Levy Syndrome Roussy-Levy Disease Roussy-Levy Hereditary Areflexic Dystasia Syndrome, Roussy-Levy |
| Concept UI |
M0336505 |
| Preferred term | Hereditary Type I Motor and Sensory Neuropathy |
| Entry term(s) |
Charcot Marie Tooth Disease, Type I Charcot-Marie-Tooth Disease, Type I HMN Distal Type I HMSN I HMSN Type I Hereditary Motor, and Sensory Neuropathy Type I Neuropathy, Type I Hereditary Motor and Sensory |
| Concept UI |
M0023765 |
| Preferred term | HMSN Type II |
| Entry term(s) |
Charcot Marie Tooth Disease, Type II Charcot-Marie-Tooth Disease, Type II HMSN II Hereditary Motor and Sensory Neuropathy Type II Hereditary Motor and Sensory-Neuropathy Type II Neuropathy, Type II Hereditary Motor and Sensory |
| Concept UI |
M0336970 |
| Preferred term | Charcot-Marie-Tooth Disease, Type IA |
| Entry term(s) |
Charcot Marie Tooth Disease, Type 1A Charcot Marie Tooth Disease, Type IA Charcot Marie Tooth Neuropathy, Type 1A Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A Charcot-Marie-Tooth Disease, Demyelinating, Type 1A Charcot-Marie-Tooth Disease, Type 1A Charcot-Marie-Tooth Neuropathy, Type 1A HMSN 1A HMSN IA HMSN1A Hereditary Motor and Sensory Neuropathy 1A Hereditary Motor and Sensory Neuropathy IA |
| Concept UI |
M0336971 |
| Preferred term | Charcot-Marie-Tooth Disease, Type IB |
| Entry term(s) |
Charcot Marie Tooth Disease, Type 1B Charcot Marie Tooth Disease, Type IB Charcot Marie Tooth Neuropathy, Type 1B Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B Charcot-Marie-Tooth Disease, Demyelinating, Type 1B Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy Charcot-Marie-Tooth Disease, Type 1B Charcot-Marie-Tooth Neuropathy, Type 1B HMSN 1B HMSN IB HMSN1B Hereditary Motor And Sensory Neuropathy IB Hereditary Motor and Sensory Neuropathy 1B |
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