Hereditary spastic paraplegia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SPASTIC PARAPLEGIA, HEREDITARY
C0037773
ZFYVE26 Unknown — Disgenet —
All101 Causal0 Unknown101
Related Diseases Diseases that share the most curated genes with Hereditary spastic paraplegia.
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Spastic paraplegia 67 shared genesNIPA1, ABCD1, ALDH18A1, SLC16A2, ALS2, AP4M1, ARSI, MTRFR, SETX, SPG11, USP8, UCHL1 +55 more Related via 67 shared genes including NIPA1, ABCD1, ALDH18A1. Spastic ataxia 14 shared genesSETX, SPG11, PNPLA6, CYP7B1, KIF1C, SACS, SPG7, SPAST, KIF1A, AMPD2, FA2H, C19orf12 +2 more Related via 14 shared genes including SETX, SPG11, PNPLA6. Charcot-marie-tooth disease 16 shared genesSETX, SPG11, NRG1, BICD2, KIF5A, SH3TC2, BSCL2, POLG, REEP1, PLEKHG5, DNM2, TFG +4 more Related via 16 shared genes including SETX, SPG11, NRG1. complex hereditary spastic paraplegia 7 shared genesNT5C2, B4GALNT1, GBA2, DSTYK, VPS37A, ENTPD1, MAG Related via 7 shared genes including NT5C2, B4GALNT1, GBA2. Congenital neurologic anomalies 13 shared genesABCD1, RNASEH2B, ALDH18A1, AP4M1, AP4B1, AP4E1, POLG, CYP2U1, AMPD2, ATL1, GJC2, ERLIN2 +1 more Related via 13 shared genes including ABCD1, RNASEH2B, ALDH18A1.