Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: KIF1A related neurological disorder · Hereditary sensory and autonomic neuropathy type 2
Neuropathy, hereditary sensory, type 2C
Any hereditary sensory and autonomic neuropathy type 2 in which the cause of the disease is a mutation in the KIF1A gene.
This condition has no sub-types.