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(e.g. rs7903146, CYP51, nitric oxide metabolic process, Pseudomonas infection, Retina)
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QuickView for hydrocephalus (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. L1CAM
  2. DEL8Q12Q21
  3. PIK3R2
  4. MPDZ
  5. CCND2
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. Zinc finger C2H2 superfamily
  2. Zinc finger C2H2-type
  3. RNA polymerase II regulatory region sequence-specific DNA binding
  4. RNA polymerase II regulatory region DNA binding
  5. transcription regulatory region sequence-specific DNA binding
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Curated Studies

Most Correlated Studies

  1. OMIM - Congenital disorder
  2. OMIM - Hydrocephalus
  3. OMIM - Disorder of brain
  4. OMIM - Multiple congenital anomalies
  5. Mouse Phenotypes - Hydrocephalus
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Literature

Most Relevant Literature

  1. Hydrocephalus].
  2. Normal Pressure Hydrocephalus Associated with Alzheimer's Disease.
  3. Neurobehavioural changes and morphological study of cerebellar purkinje cells in kaolin induced hydr…
  4. Blood-brain barrier leakage of blood proteins in idiopathic normal pressure hydrocephalus.
  5. AQP4 autoantibodies in patients with idiopathic normal pressure hydrocephalus.
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Clinical Trials

Most Relevant Clinical Trials

  1. Cerebrospinal Fluid Proteome in Hydrocephalus
  2. Normal Pressure Hydrocephalus and Sleep Apnea
  3. Noninvasive Intracranial Pressure and Hydrocephalus Patients
  4. Isoflurane-induced Neuroinflammation in Children With Hydrocephalus
  5. Anterior Pituitary Function in Patients With Hydrocephalus
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