complex hereditary spastic paraplegia

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
complex hereditary spastic paraplegia
B4GALNT1 Unknown — ClinGen
DSTYK Unknown — ClinGen —
ENTPD1 Unknown — ClinGen
GBA2 Unknown — ClinGen
MAG Unknown — ClinGen
NT5C2 Unknown — ClinGen
VPS37A Unknown — ClinGen
All7 Causal0 Unknown7
Related Diseases Diseases that share the most curated genes with complex hereditary spastic paraplegia.
5 View disease cluster →
Paraplegia 1 shared geneVPS37A Related via 1 shared gene including VPS37A. Hereditary spastic paraplegia 7 shared genesNT5C2, B4GALNT1, GBA2, DSTYK, VPS37A, ENTPD1, MAG Related via 7 shared genes including NT5C2, B4GALNT1, GBA2. Spastic paraplegia 7 shared genesNT5C2, B4GALNT1, GBA2, DSTYK, VPS37A, ENTPD1, MAG Related via 7 shared genes including NT5C2, B4GALNT1, GBA2. Congenital anomalies of kidney and urinary tract 1 shared geneDSTYK Related via 1 shared gene including DSTYK. Polyneuropathy 1 shared geneGBA2 Related via 1 shared gene including GBA2.