Distal axonal motor neuropathy-myofibrillar myopathy syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
AUTOSOMAL DOMINANT DISTAL AXONAL MOTOR NEUROPATHY, MYOFIBRILLAR MYOPATHY SYNDROME
C5568137
HSPB8 Unknown — Disgenet
AUTOSOMAL DOMINANT DISTAL AXONAL MOTOR NEUROPATHY-MYOFIBRILLAR MYOPATHY SYNDROME
MONDO:0018773
HSPB8 Unknown
26718575
ClinVar
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Distal axonal motor neuropathy-myofibrillar myopathy syndrome.
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neuronopathy, distal hereditary motor, autosomal dominant 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.