Charcot-Marie-Tooth Disease, Demyelinating, Type 1c (CMT1C)

Alias:

Charcot-Marie-Tooth Disease Type 1c

Charcot-Marie-Tooth Disease, Type 1c

Cmt1c

Hmsn Ic

Hmsn1c

Charcot-Marie-Tooth Neuropathy Type 1c

Neuropathy, Hereditary Motor and Sensory, Type Ic

Charcot-Marie-Tooth Disease Demyelinating Type 1c

Neuropathy Hereditary Motor and Sensory Type 1c

Charcot-Marie-Tooth Disease, Demyelinating, 1c

Hereditary Motor and Sensory Neuropathy Ic

Charcot-Marie-Tooth Neuropathy, Type 1c

Charcot-Marie-Tooth Disease, Type Ic

Cmt, Slow Nerve Conduction Type C

Cmt Slow Nerve Conduction Type C

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Charcot-Marie-Tooth Disease, Demyelinating, Type 1c, also known as charcot-marie-tooth disease type 1c, is related to polyneuropathy and tooth disease. An important gene associated with Charcot-Marie-Tooth Disease, Demyelinating, Type 1c is LITAF (Lipopolysaccharide Induced TNF Factor), and among its related pathways/superpathways are Intracellular trafficking proteins involved in CMT neuropathy and EGR2 and SOX10-mediated initiation of Schwann cell myelination. Affiliated tissues include peripheral nerve, and related phenotypes are decreased nerve conduction velocity and decreased motor nerve conduction velocity

Related ID：

MALACARDS：CHR647

OMIM：601098

MESH：C537984