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Spastic paraplegia 10, autosomal dominant
Spastic paraplegia 10, autosomal dominant
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Subtype of:
Spastic paraplegia
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(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 10, autosomal dominant
MONDO_0011408
KIF5A
Unknown
29954873
29566793
12355402
25352184
18203753
16476820
21107874
18853458
18245137
15452312
16489470
Open Targets
Endocytosis
Dopaminergic synapse
Motor proteins
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Salmonella infection
Non-small cell lung cancer
MHC class II antigen presentation
RHO GTPases activate KTN1
COPI-dependent Golgi-to-ER retrograde traffic
Kinesins
+12 more
Spastic paraplegia 10, autosomal dominant or pseudoautosomal, NOT imprinted
MONDO_0011408
KIF5A
Unknown
16476820
12355402
Open Targets
Endocytosis
Dopaminergic synapse
Motor proteins
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Salmonella infection
Non-small cell lung cancer
MHC class II antigen presentation
RHO GTPases activate KTN1
COPI-dependent Golgi-to-ER retrograde traffic
Kinesins
+12 more
All
1
Causal
0
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
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Amyotrophic lateral sclerosis, susceptibility to, 25
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
Inherited neurodegenerative disorder
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
Severe neonatal myoclonus
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
Genetic neurodegenerative disease
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
Frontotemporal dementia with or without amyotrophic lateral sclerosis
1 shared gene
KIF5A
Related via 1 shared gene including KIF5A.
1
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