Spastic paraplegia 12, autosomal dominant

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Subtype of: Spastic paraplegia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Spastic paraplegia 12, autosomal dominant
MONDO_0011489
RTN2 Unknown
22232211 28362824 24123792 38527963 35684947
Open Targets —
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Spastic paraplegia 12, autosomal dominant.
5 View disease cluster →
Lower limb spasticity 1 shared geneRTN2 Related via 1 shared gene including RTN2. Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity 1 shared geneRTN2 Related via 1 shared gene including RTN2. Distal hereditary motor neuropathy 1 shared geneRTN2 Related via 1 shared gene including RTN2. Hereditary spastic paraplegia 1 shared geneRTN2 Related via 1 shared gene including RTN2. Spastic paraplegia 1 shared geneRTN2 Related via 1 shared gene including RTN2.