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hereditary spastic paraplegia 35
hereditary spastic paraplegia 35
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
hereditary spastic paraplegia 35
FA2H
Causal
31837835
22965561
21592092
30446360
ClinGen
Sphingolipid de novo biosynthesis
All
1
Causal
1
Unknown
0
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
1
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Neurodegeneration with brain iron accumulation
1 shared gene
FA2H
Related via 1 shared gene including FA2H.
Cerebellar atrophy
1 shared gene
FA2H
Related via 1 shared gene including FA2H.
Spastic ataxia
1 shared gene
FA2H
Related via 1 shared gene including FA2H.
Hereditary spastic paraplegia
1 shared gene
FA2H
Related via 1 shared gene including FA2H.
Spastic paraplegia
1 shared gene
FA2H
Related via 1 shared gene including FA2H.
1
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