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Disease Charcot-Marie-Tooth Disease

Name Charcot-Marie-Tooth Disease
Synonyms Areflexic Dystasia, Hereditary | Areflexic Dystasias, Hereditary | Atrophies, Peroneal Muscular | Atrophy, Muscular, Peroneal | Atrophy, Peroneal Muscular | Charcot Marie Disease | Charcot-Marie Disease | Charcot Marie Tooth 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 1A | Charcot Marie Tooth Disease, Type 1B | Charcot-Marie-Tooth Disease, Type 1B | Charcot Marie Tooth Disease, Type I | Charcot-Marie-Tooth Disease, Type I | Charcot Marie Tooth Disease, Type IA | Charcot-Marie-Tooth Disease, Type IA | Charcot Marie Tooth Disease, Type IB | Charcot-Marie-Tooth Disease, Type IB | Charcot Marie Tooth Disease, Type II | Charcot-Marie-Tooth Disease, Type II | Charcot Marie Tooth Hereditary Neuropathy | Charcot-Marie-Tooth Hereditary Neuropathy | Charcot Marie Tooth Neuropathy, Type 1A | Charcot-Marie-Tooth Neuropathy, Type 1A | Charcot Marie Tooth Neuropathy, Type 1B | Charcot-Marie-Tooth Neuropathy, Type 1B | Charcot Marie Tooth Syndrome | Charcot-Marie-Tooth Syndrome | CMT1A | CMT1B | Dystasia, Hereditary Areflexic | Dystasias, Hereditary Areflexic | Hereditary Areflexic Dystasia | Hereditary Areflexic Dystasias | Hereditary Motor and Sensory Neuropathy 1A | Hereditary Motor and Sensory Neuropathy 1B | HEREDITARY MOTOR AND SENSORY NEUROPATHY I | Hereditary Motor and Sensory Neuropathy IA | Hereditary Motor And Sensory Neuropathy IB | Hereditary Motor, and Sensory Neuropathy Type I | Hereditary Motor and Sensory Neuropathy Type II | Hereditary Motor and Sensory-Neuropathy Type II | Hereditary Neuropathy, Charcot-Marie-Tooth | Hereditary Type I Motor and Sensory Neuropathy | HMN Distal Type I | HMSN1 | HMSN1A | HMSN 1A | HMSN1B | HMSN 1B | HMSN I | HMSN IA | HMSN IB | HMSN II | HMSN Type I | HMSN Type II | 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 Disease | Roussy Levy Hereditary Areflexic Dystasia | Roussy-Levy Hereditary Areflexic Dystasia | Roussy Levy Syndrome | Roussy-Levy Syndrome | Syndrome, Charcot-Marie-Tooth | Syndrome, Roussy-Levy
Definition 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)
Categories Congenital abnormality | Genetic disease (inborn) | Nervous system disease
MeSH® ID D002607
OMIM® IDs 118200 | 118220 | 180800
External Links

Top ↑ Ancestors

1. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Nervous System Malformations Has associated chemicals Has associated genes Has associated exposure references Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Charcot-Marie-Tooth Disease Has associated chemicals Has associated genes
2. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neurodegenerative Diseases Has associated chemicals Has associated genes Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Charcot-Marie-Tooth Disease Has associated chemicals Has associated genes
3. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neuromuscular Diseases Has associated chemicals Has associated genes Has associated exposure references Peripheral Nervous System Diseases Has associated chemicals Has associated genes Polyneuropathies Has associated chemicals Has associated genes Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Charcot-Marie-Tooth Disease Has associated chemicals Has associated genes
4. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Congenital Abnormalities Has associated chemicals Has associated genes Has associated exposure references Nervous System Malformations Has associated chemicals Has associated genes Has associated exposure references Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Charcot-Marie-Tooth Disease Has associated chemicals Has associated genes
5. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Hereditary Sensory and Motor Neuropathy Has associated chemicals Has associated genes Charcot-Marie-Tooth Disease Has associated chemicals Has associated genes

Top ↑ Descendants

Charcot-Marie-Tooth Disease Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease and deafness
  Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Has associated chemicals Has associated genes
  Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Has associated chemicals Has associated genes
  CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Has associated chemicals Has associated genes
  Charcot-Marie-Tooth Disease, Axonal, Type 2n Has associated chemicals Has associated genes
  Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, dominant intermediate 1
  Charcot-Marie-Tooth disease, dominant intermediate 2
  Charcot-Marie-Tooth disease, dominant intermediate 3
  Charcot-Marie-Tooth Disease, Dominant Intermediate A
  Charcot-Marie-Tooth Disease, Dominant Intermediate B Has associated chemicals Has associated genes
  Charcot-Marie-Tooth Disease, Dominant Intermediate C Has associated chemicals Has associated genes
  Charcot-Marie-Tooth Disease, Dominant Intermediate D Has associated chemicals Has associated genes
  Charcot-Marie-Tooth Disease, Foot Deformity of
  Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type
  Charcot-Marie-Tooth Disease, Recessive Intermediate A Has associated chemicals Has associated genes
  CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 1C Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 1D Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 1E
  Charcot-Marie-Tooth disease, Type 1F Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2A
  Charcot-Marie-Tooth disease, Type 2B Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2B1 Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2B2 Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2C
  Charcot-Marie-Tooth disease, Type 2D Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2E Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2F Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2G Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2H
  Charcot-Marie-Tooth disease, Type 2I Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2J Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 2K Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 4A Has associated chemicals Has associated genes
View node Charcot-Marie-Tooth disease, Type 4A, axonal form Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 4B1 Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 4B2 Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 4B2, with early-onset glaucoma
  Charcot-Marie-Tooth disease, Type 4C Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, Type 4E Has associated chemicals Has associated genes
  Charcot-Marie-Tooth Disease, Type 4H Has associated chemicals Has associated genes
  Charcot-Marie-Tooth Disease, Type 4j Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease with ptosis and parkinsonism
  Charcot-Marie-Tooth disease, X-linked, 1 Has associated chemicals Has associated genes
  Charcot-Marie-Tooth disease, X-linked recessive, 2
  Charcot-Marie-Tooth disease, X-linked recessive, 3
  Charcot-Marie-Tooth Neuropathy, Dominant Intermediate B, with Neutropenia
  Charcot-Marie-Tooth Neuropathy, Type 4B2, with Early-Onset Glaucoma
  Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined
  Charcot Marie Tooth type 1 aplasia cutis congenita
  Cowchock syndrome Has associated chemicals Has associated genes
  Hereditary Motor And Sensory Neuropathy, Type IIC Has associated chemicals Has associated genes
  Keratoderma palmoplantar spastic paralysis
  Neuropathy, Distal Hereditary Motor, Type IIA Has associated chemicals Has associated genes
  Neuropathy, hereditary motor and sensory, LOM type Has associated chemicals Has associated genes
  Polyneuropathy, Mixed, of Early Onset