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Spastic paraplegia 26, autosomal recessive
Spastic paraplegia 26, autosomal recessive
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Subtype of:
Spastic paraplegia
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Spastic paraplegia 26, autosomal recessive
MONDO_0012213
B4GALNT1
Unknown
23746551
24103911
24283893
Open Targets
Sphingolipid metabolism
Glycosphingolipid biosynthesis - ganglio series
Metabolic pathways
Glycosphingolipid metabolism
+1 more
SPG26
MONDO_0012213
B4GALNT1
Unknown
23746551
Open Targets
Sphingolipid metabolism
Glycosphingolipid biosynthesis - ganglio series
Metabolic pathways
Glycosphingolipid metabolism
+1 more
All
1
Causal
0
Unknown
1
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Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
Related Diseases
Diseases that share the most curated genes with Spastic paraplegia 26, autosomal recessive.
5
View disease cluster →
Complex hereditary spastic paraplegia
1 shared gene
B4GALNT1
Related via 1 shared gene including B4GALNT1.
Immune system disease
1 shared gene
B4GALNT1
Related via 1 shared gene including B4GALNT1.
Hereditary spastic paraplegia
1 shared gene
B4GALNT1
Related via 1 shared gene including B4GALNT1.
Spastic paraplegia
1 shared gene
B4GALNT1
Related via 1 shared gene including B4GALNT1.
Autism
1 shared gene
B4GALNT1
Related via 1 shared gene including B4GALNT1.
1
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