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Charcot-Marie-Tooth Disease
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease 2 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease ∟ ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease ∟ ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease ∟ ∟ ∟ ∟ ∟ ∟ Charcot-Marie-Tooth Disease |
historyNote*: | 2000(1966)
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publicMeSHNote*: | 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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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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activeMeSHYear*: | |
dateCreated*: | 1999-11-08X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Charcot-Marie-Toothin tauti (fi) XHereditaarinen motoris-sensorinen neuropatia (fi, replaced) HMSN (fi, replaced) Charcot-Marien tauti (fi, replaced) Charcot-Marien neuropatia (fi, replaced) Charcot-Marie-Toothin neuropatia (fi, replaced) Peroneaalinen lihasatrofia (fi, replaced) Charcot-Marie-Tooths sjukdom (sv) HMSN typ I (sv, replaced) HMSN typ II (sv, replaced) CMT (sv, replaced) Peroneal Muscular Atrophy (en, replaced) Neuropathy, Type II Hereditary Motor and Sensory (en, replaced) Hereditary Motor and Sensory-Neuropathy Type II (en, replaced) Hereditary Motor, and Sensory Neuropathy Type I (en, replaced) Charcot-Marie-Tooth Disease, Type II (en, replaced) Charcot-Marie-Tooth Disease, Type I (en, replaced) Charcot-Marie Disease (en, replaced) HMN Distal Type I (en, replaced) HMSN I (en, replaced) Neuropathy, Type I Hereditary Motor and Sensory (en, replaced) Muscular Atrophy, Peroneal (en, replaced) HMSN Type I (en, replaced) HMSN II (en, replaced) Atrophy, Muscular, Peroneal (en, replaced) Atrophia musculorum peroneorum (la-FI, replaced) Morbus Charcot-Marie-Tooth (la-FI, replaced) Morbus Charcot-Marie (la-FI, replaced) |
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