Charcot-Marie-Tooth disease dominant intermediate E

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Charcot-Marie-Tooth disease dominant intermediate E
INF2 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Charcot-Marie-Tooth disease dominant intermediate E.
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Hereditary motor and sensory neuropathy 1 shared geneINF2 Related via 1 shared gene including INF2. Idiopathic steroid-resistant nephrotic syndrome 1 shared geneINF2 Related via 1 shared gene including INF2. Focal segmental glomerulosclerosis 1 shared geneINF2 Related via 1 shared gene including INF2. Genetic steroid-resistant nephrotic syndrome 1 shared geneINF2 Related via 1 shared gene including INF2. Hereditary steroid-resistant nephrotic syndrome 1 shared geneINF2 Related via 1 shared gene including INF2.