Charcot-Marie-Tooth Disease Type 1g

Charcot-Marie-Tooth Disease Type 1g(来自ICD-11)

别称:

Pmp2-Related Hereditary Motor and Sensory Neuropathy Type 1

Pmp2-Related Charcot-Marie-Tooth Neuropathy Type 1

Pmp2-Related Charcot-Marie-Tooth Disease Type 1

Pmp2-Related Cmt1

Cmt1g

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Charcot-Marie-Tooth Disease Type 1g, also known as pmp2-related hereditary motor and sensory neuropathy type 1, is related to charcot-marie-tooth disease, demyelinating, type 1g and charcot-marie-tooth disease, x-linked recessive, 2. An important gene associated with Charcot-Marie-Tooth Disease Type 1g is PMP2 (Peripheral Myelin Protein 2), and among its related pathways/superpathways is Intracellular trafficking proteins involved in CMT neuropathy.

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