Neuropathy, hereditary motor and sensory, type 6B
MONDO:0014671Any hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the SLC25A46 gene.
Also known as: CMT6B, Charcot-Marie-Tooth disease, type 6B, HMSN 6B, HMSN6B, SLC25A46 hereditary motor and sensory neuropathy type 6, hereditary motor and sensory neuropathy type 6 caused by mutation in SLC25A46, neuropathy, hereditary motor and sensory, type 6B, neuropathy, hereditary motor and sensory, type VIB
7 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(680)
Nervous system disorder
(231)
Hereditary disease
(176)
Peripheral nervous system disorder
(114)
Neuromuscular disease
(106)
Peripheral neuropathy
(91)
Human disease
(14)
Hereditary neurological disease
(6)
Hereditary peripheral neuropathy
(6)
Hereditary motor and sensory neuropathy
(3)