Epilepsy

The following 50 diseases are displayed in order of most significant enrichment p-value relative to Epilepsy. Download all relationships search
Seizures p-value: 3.0878729101489e-258 172 genes   common genes
Neurologic Manifestations p-value: 1.32417858278298e-157 1705 genes   common genes
Epilepsies, Partial p-value: 2.77300830677774e-120 84 genes   common genes
Mental Disorders p-value: 1.85790411714306e-94 2238 genes   common genes
Neurobehavioral Manifestations p-value: 1.87142656380625e-87 713 genes   common genes
Mental Disorders Diagnosed in Childhood p-value: 3.13115694048773e-87 885 genes   common genes
Epilepsy, Temporal Lobe p-value: 8.16669084272334e-84 59 genes   common genes
Movement Disorders p-value: 5.20257938171915e-78 761 genes   common genes
Substance-Related Disorders p-value: 1.32652940516203e-73 474 genes   common genes
Neurodegenerative Diseases p-value: 1.12761708848174e-66 1618 genes   common genes
Cognition Disorders p-value: 2.04076246034554e-62 333 genes   common genes
Dyskinesias p-value: 3.57606273410495e-60 417 genes   common genes
Alcohol-Related Disorders p-value: 2.86808814442365e-54 247 genes   common genes
Basal Ganglia Diseases p-value: 5.74884966488423e-54 496 genes   common genes
Dementia p-value: 1.87286436950613e-52 826 genes   common genes
Pain p-value: 7.0365093224266e-51 369 genes   common genes
Brain Ischemia p-value: 2.50413313132253e-50 476 genes   common genes
Tauopathies p-value: 3.98581250194174e-50 672 genes   common genes
Alzheimer Disease p-value: 7.17041822349419e-50 664 genes   common genes
Heredodegenerative Disorders, Nervous System p-value: 4.90167008575039e-48 754 genes   common genes
Genetic Diseases, Inborn p-value: 3.86269777620149e-47 2862 genes   common genes
Craniocerebral Trauma p-value: 2.00121450599615e-46 151 genes   common genes
Cerebrovascular Disorders p-value: 2.30128805630579e-45 706 genes   common genes
Schizophrenia p-value: 2.72183297558011e-45 506 genes   common genes
Brain Injuries p-value: 3.55481511921631e-45 122 genes   common genes
Communication Disorders p-value: 8.22374703905162e-45 179 genes   common genes
Mood Disorders p-value: 8.09943052135174e-44 392 genes   common genes
Trauma, Nervous System p-value: 4.91198997177725e-43 240 genes   common genes
Parkinsonian Disorders p-value: 9.59111197945005e-43 363 genes   common genes
Sleep Disorders p-value: 6.76773858370622e-42 153 genes   common genes
Nutrition Disorders p-value: 1.06925864558588e-41 801 genes   common genes
Pregnancy Complications p-value: 1.84174382953382e-41 803 genes   common genes
Stroke p-value: 4.42046163747907e-41 388 genes   common genes
Central Nervous System Infections p-value: 1.39113323371949e-40 371 genes   common genes
Central Nervous System Viral Diseases p-value: 2.90255178092705e-40 293 genes   common genes
Brain Infarction p-value: 5.21382991652718e-40 380 genes   common genes
Cerebral Infarction p-value: 5.21382991652718e-40 380 genes   common genes
Neurotoxicity Syndromes p-value: 1.84275209828764e-39 108 genes   common genes
Alcoholism p-value: 1.9818682107384e-39 163 genes   common genes
Spinal Cord Diseases p-value: 2.82043826851644e-39 428 genes   common genes
Parkinson Disease p-value: 4.58807053391952e-39 325 genes   common genes
Memory Disorders p-value: 5.5390284780519e-39 94 genes   common genes
Peripheral Nervous System Diseases p-value: 8.3369047963309e-39 437 genes   common genes
Congenital Abnormalities p-value: 8.96895196652827e-39 1817 genes   common genes
Neuromuscular Diseases p-value: 1.04153072627136e-37 1015 genes   common genes
Infant, Newborn, Diseases p-value: 3.98472906371217e-37 399 genes   common genes
Malnutrition p-value: 1.66765934326759e-36 302 genes   common genes
Prenatal Exposure Delayed Effects p-value: 1.95660336208594e-36 83 genes   common genes
Metabolic Diseases p-value: 2.0101825870526e-36 2535 genes   common genes
Encephalitis p-value: 2.7284827160379e-36 242 genes   common genes

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The Wall Lab is in the Center for Biomedical Informatics at Harvard Medical School, on the fourth floor of the Countway Medical Library. We are translational bioinformaticians working on strategies to understand, diagnose, and treat complex human diseases, chiefly including autism.

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Grasping the genetic complexity of autism is a monumental effort that will require unprecendented amounts of information. We are in the process of raising funds to gather this information. If you are interested in learning more about how to contribute to our mission, please contact us.
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