Charcot-Marie-Tooth disease type 2C (Q104270): Difference between revisions
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Revision as of 10:08, 17 August 2026
Autosomal dominant Charcot-Marie-Tooth disease type 2C (CMT2C) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by the association of vocal cord anomalies, impairment of respiratory muscles and sensorineural hearing loss with the distal hands and feet weakness. Onset is between infancy and the 6th decade.
| Language | Label | Description | Also known as |
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| default for all languages | ID_2074400987 |
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| English | Charcot-Marie-Tooth disease type 2C |
Autosomal dominant Charcot-Marie-Tooth disease type 2C (CMT2C) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by the association of vocal cord anomalies, impairment of respiratory muscles and sensorineural hearing loss with the distal hands and feet weakness. Onset is between infancy and the 6th decade. |
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CID11:ID_2074400987
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