Charcot-Marie-Tooth disease 1 autosomal recessive (Q92289): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Doença de Charcot-Marie-Tooth tipo 4 (CMT4) pertence ao grupo geneticamente heterogêneo das doenças da polineuropatia periférica sensitivomotora de Charcot-Marie-Tooth. Inclui formas autossômicas recessivas e desmielinizantes da doença de Charcot-Marie-Toote. | |||
| description / en | description / en | ||
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. | |||
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. |
