Charcot-Marie-Tooth disease type 2K (Q104260): Difference between revisions
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16 August 2026
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Latest revision as of 10:07, 17 August 2026
Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy. CMT2K is a rare form of CMT with a mild phenotype, onset during the second decade of life and very slow progression.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1720211658 |
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| English | Charcot-Marie-Tooth disease type 2K |
Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy. CMT2K is a rare form of CMT with a mild phenotype, onset during the second decade of life and very slow progression. |
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CID11:ID_1720211658
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dki-india-ID_1720211658
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Concluído
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16 August 2026
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