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Neuropathy, hereditary motor and sensory, type 6B

rare

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

Identifiers
MONDO:0014671 OMIM:616505
Causal genes
SLC25A46
Part of
Hereditary motor and sensory neuropathy type 6Motor peripheral neuropathy
Also known as
Charcot-Marie-Tooth disease, type 6B · CMT6B · hereditary motor and sensory neuropathy type 6 caused by mutation in SLC25A46 · HMSN 6B · HMSN6B

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