Neuronopathy, distal hereditary motor, autosomal dominant

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Subtype of: Distal hereditary motor neuropathy · Neuronopathy, distal hereditary motor
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neuronopathy, distal hereditary motor, autosomal dominant
MONDO_0010839
TRPV4 Causal
22526352 22702953 20037588 20037586 20037587 21288981 25256292
Open Targets
All9 Causal1 Unknown8
Related Diseases Diseases that share the most curated genes with Neuronopathy, distal hereditary motor, autosomal dominant.
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Distal axonal motor neuropathy-myofibrillar myopathy syndrome 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. Vacuolar myopathy 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. Distal muscular dystrophy 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. Distal spinal muscular atrophy 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. Distal hereditary motor neuropathy 1 shared geneHSPB8 Related via 1 shared gene including HSPB8.