Spastic paraplegia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SPASTIC PARAPLEGIA 93, AUTOSOMAL RECESSIVE
620938MONDO:0975796
NFU1 Causal — ClinVar, HPO —
All120 Causal51 Unknown106
Related Diseases Diseases that share the most curated genes with Spastic paraplegia.
5 View disease cluster →
Hereditary 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 16 shared genesSETX, SPG11, PNPLA6, CYP7B1, VAMP1, KIF1C, SACS, SPG7, SPAST, KIF1A, AMPD2, FA2H +4 more Related via 16 shared genes including SETX, SPG11, PNPLA6. Congenital neurologic anomalies 13 shared genesABCD1, ALDH18A1, AP4M1, SETBP1, AP4B1, AP4E1, MCOLN1, SMC1A, CYP2U1, AMPD2, ATL1, GJC2 +1 more Related via 13 shared genes including ABCD1, ALDH18A1, AP4M1. complex hereditary spastic paraplegia 7 shared genesNT5C2, B4GALNT1, GBA2, DSTYK, VPS37A, ENTPD1, MAG Related via 7 shared genes including NT5C2, B4GALNT1, GBA2. Dysarthria 7 shared genesPNPLA6, ZGRF1, SPG7, SMC1A, SPART, BIVM-ERCC5, ERCC5 Related via 7 shared genes including PNPLA6, ZGRF1, SPG7.