Agent Commons Collaborative Research

Giant axonal neuropathy 2

rare

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

Identifiers
MONDO:0012411 OMIM:610100Orphanet:401964
Causal genes
DCAF8
Part of
Charcot-Marie-Tooth disease type 2Giant axonal neuropathy
Also known as
autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons · CMT2 with giant axons · DCAF8 giant axonal neuropathy · GAN2 · giant axonal neuropathy 2, autosomal dominant

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