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paraplegia
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Summary
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Genetic Markers
Most Correlated Genes
Most Correlated SNPs
SPG21
SPG16
L1CAM
BSCL2
SPOAN
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
GSE22886_DAY1_VS_DAY7_MONOCYTE_IN_CULTURE_DN
GSE15330_HSC_VS_LYMPHOID_PRIMED_MULTIPOTENT_PROGENITOR_DN
KIM_ALL_DISORDERS_OLIGODENDROCYTE_NUMBER_CORR_UP
cytosol
mitochondrial membrane
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Curated Studies
Most Correlated Studies
CD4+ T cells of human T lymphotropic virus type I (HTLV-1) infected individuals
PBMCs of myelopathy/tropical spastic paraparesis patients treated with Fas agonist/antagonist mAbs
OMIM - Brain CNS Motor Neuron and other Neuropathy Disorders
OMIM - Spastic Ataxias
OMIM - Spastic paraplegia
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Literature
Most Relevant Literature
A novel homozygous synonymous splicing variant in SELENOI gene causes spastic paraplegia 81.
Post-thoracotomy paraplegia after oxidized cellulose spinal compression.
Paraplegia secondary to disseminated mucormycosis: case report and literature review.
A case of spastic paraplegia with SPG4 and SPG3 associated mutations].
Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spast…
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Clinical Trials
Most Relevant Clinical Trials
Physiotherapy in Hereditary Spastic Paraplegia
A Registered Cohort Study on Spastic Paraplegia
The ReWalk Exoskeletal Walking System for Persons With Paraplegia
Gait Training for Individuals With Paraplegia Using the H-MEX Exoskeleton
Effects of Botulinum Toxin Injections in Patients With Hereditary Spastic Paraplegia
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