Spastic paraplegia 73, 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 73, autosomal dominant
MONDO_0014568
CPT1C Unknown
30911584 30564185 25751282
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Spastic paraplegia 73, autosomal dominant.
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Panic disorder 1 shared geneCPT1C Related via 1 shared gene including CPT1C. Peripheral nervous system disease 1 shared geneCPT1C Related via 1 shared gene including CPT1C. Non-neoplastic peripheral nervous system disease 1 shared geneCPT1C Related via 1 shared gene including CPT1C. Hereditary spastic paraplegia 1 shared geneCPT1C Related via 1 shared gene including CPT1C. Spastic paraplegia 1 shared geneCPT1C Related via 1 shared gene including CPT1C.