Charcot-Marie-Tooth disease 1 autosomal recessive (Q92289): Difference between revisions
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Revision as of 07:26, 16 August 2026
Charcot-Marie-Tooth disease type 4 (CMT4) belongs to the genetically heterogeneous group of Charcot-Marie-Tooth peripheral sensorimotor polyneuropathy diseases. It includes autosomal recessive, demyelinating forms of Charcot-Marie-Toothe disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_220263794 |
||
| English | Charcot-Marie-Tooth disease 1 autosomal recessive |
Charcot-Marie-Tooth disease type 4 (CMT4) belongs to the genetically heterogeneous group of Charcot-Marie-Tooth peripheral sensorimotor polyneuropathy diseases. It includes autosomal recessive, demyelinating forms of Charcot-Marie-Toothe disease. |
Statements
CID11:ID_220263794
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dki-india-ID_220263794
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Concluído
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