Charcot-Marie-Tooth disease type 1A

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Charcot-Marie-Tooth disease type 1A
PMP22 Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Charcot-Marie-Tooth disease type 1A.
5 View disease cluster →
Hereditary neuropathy with liability to pressure palsies 1 shared genePMP22 Related via 1 shared gene including PMP22. Paresthesia 1 shared genePMP22 Related via 1 shared gene including PMP22. Hereditary sensory and motor neuropathy 1 shared genePMP22 Related via 1 shared gene including PMP22. Demyelinating diseases 1 shared genePMP22 Related via 1 shared gene including PMP22. Myoclonic epilepsy 1 shared genePMP22 Related via 1 shared gene including PMP22.