Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a (CMT2A2A)

Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a(来自ICD-11)

别称:

Cmt2a2

Charcot-Marie-Tooth Disease, Axonal, Type 2a2

Hereditary Motor and Sensory Neuropathy Iia2

Hmsn Iia2

Cmt2a2a

Hmsn2a2

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2a2

Charcot-Marie-Tooth Disease, Neuronal, Type 2a2

Charcot-Marie-Tooth Disease, Axonal, Type 2a2a

Charcot-Marie-Tooth Disease Neuronal Type 2a2

Charcot-Marie-Tooth Disease Axonal Type 2a2

Charcot-Marie-Tooth Disease, Axonal, 2a2a

Charcot-Marie-Tooth Neuropathy, Type 2a2

Charcot-Marie-Tooth Neuropathy Type 2a2

Charcot-Marie-Tooth Disease, Type 2a2a

Charcot-Marie-Tooth Disease Type 2a2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a, also known as cmt2a2, is related to charcot-marie-tooth disease type 2a2a and charcot-marie-tooth disease, demyelinating, type 1b, and has symptoms including pain An important gene associated with Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a is MFN2 (Mitofusin 2). Affiliated tissues include spinal cord and brain, and related phenotypes are foot dorsiflexor weakness and emg: chronic denervation signs

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