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neuropathy, hereditary motor and sensory, type 6B | RareConnect | RareConnect.io

/motor peripheral neuropathy

/hereditary motor and sensory neuropathy type 6

/neuropathy, hereditary motor and sensory, type 6B

neuropathy, hereditary motor and sensory, type 6B

Rare Disease

MONDO:0014671

Also Known As

CMT6BCharcot-Marie-Tooth disease, type 6BHMSN 6BHMSN6BSLC25A46 hereditary motor and sensory neuropathy type 6hereditary motor and sensory neuropathy type 6 caused by mutation in SLC25A46neuropathy, hereditary motor and sensory, type 6Bneuropathy, hereditary motor and sensory, type VIB

Definition

Any hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the SLC25A46 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:616505 ↗

GARD

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