Charcot-Marie-Tooth disease type 4D (Q104655): Difference between revisions
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Neuropatia motora e sensitiva hereditária do tipo Lom (HMSNL) é uma forma grave de doença desmielinizante de Charcot-Marie-Tooth (CMT), associada à surdez neural na maioria dos indivíduos afetados. | |||
| description / en | description / en | ||
Hereditary motor and sensory neuropathy Lom (HMSNL) is a severe form of demyelinating Charcot-Marie-Tooth (CMT) disease, associated with neural deafness in the majority of affected individuals. | |||
Revision as of 10:31, 17 August 2026
Hereditary motor and sensory neuropathy Lom (HMSNL) is a severe form of demyelinating Charcot-Marie-Tooth (CMT) disease, associated with neural deafness in the majority of affected individuals.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_616686295 |
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| English | Charcot-Marie-Tooth disease type 4D |
Hereditary motor and sensory neuropathy Lom (HMSNL) is a severe form of demyelinating Charcot-Marie-Tooth (CMT) disease, associated with neural deafness in the majority of affected individuals. |
