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QuickView for paraplegia (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. SPG21
  2. SPG16
  3. L1CAM
  4. BSCL2
  5. SPOAN
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. GSE22886_DAY1_VS_DAY7_MONOCYTE_IN_CULTURE_DN
  2. GSE15330_HSC_VS_LYMPHOID_PRIMED_MULTIPOTENT_PROGENITOR_DN
  3. KIM_ALL_DISORDERS_OLIGODENDROCYTE_NUMBER_CORR_UP
  4. cytosol
  5. mitochondrial membrane
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Disorder of extremity
  2. Comparative profiling in 13 muscle disease groups
  3. OMIM - Nervous system disorders
  4. OMIM - Neuropathy
  5. OMIM - Spastic Ataxias
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Literature

Most Relevant Literature

  1. Homozygous variant in COQ7 causes autosomal recessive hereditary spastic paraplegia.
  2. Tuberculous Paraplegia: Outcome of Operative Intervention.
  3. Post-thoracotomy paraplegia after oxidized cellulose spinal compression.
  4. A novel homozygous synonymous splicing variant in SELENOI gene causes spastic paraplegia 81.
  5. From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum a…
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Clinical Trials

Most Relevant Clinical Trials

  1. Physiotherapy in Hereditary Spastic Paraplegia
  2. A Registered Cohort Study on Spastic Paraplegia
  3. The ReWalk Exoskeletal Walking System for Persons With Paraplegia
  4. Gait Training for Individuals With Paraplegia Using the H-MEX Exoskeleton
  5. Effects of Botulinum Toxin Injections in Patients With Hereditary Spastic Paraplegia
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