Giant axonal neuropathy 2

MONDO:0012411

Any giant axonal neuropathy in which the cause of the disease is a mutation in the DCAF8 gene.

Also known as: CMT2 with giant axons, DCAF8 giant axonal neuropathy, HMSN2 with giant axons, autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons, giant axonal neuropathy caused by mutation in DCAF8, giant axonal neuropathy type 2, GAN2, autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons

9 clinical trials for this condition and its sub-types, 0 tagged with Giant axonal neuropathy 2 itself.

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↑ Charcot-Marie-Tooth disease type 2 (9) ↑ Giant axonal neuropathy (3)

Including sub-types (9) Tagged with Giant axonal neuropathy 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.