INT260051

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Context Info
Confidence 0.69
First Reported 2009
Last Reported 2009
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.69
Pain Relevance 0

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

cell adhesion (PCDH19) plasma membrane (PCDH19)
PCDH19 (Homo sapiens)
Pain Link Frequency Relevance Heat
Central nervous system 1 5.00 Very Low Very Low Very Low
Nav1.1 1 5.00 Very Low Very Low Very Low
sodium channel 1 5.00 Very Low Very Low Very Low
imagery 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Cognitive Disorder 32 100.00 Very High Very High Very High
Intellectual Impairment 12 99.04 Very High Very High Very High
Epilepsy 38 98.12 Very High Very High Very High
Syndrome 70 91.28 High High
Partial Seizures 2 82.08 Quite High
Convulsion 28 76.72 Quite High
Fever 7 70.32 Quite High
Myoclonic Epilepsies 2 70.08 Quite High
Myoclonus 6 63.16 Quite High
Encephalopathy 6 50.00 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Mutations in PCDH19 were recently reported to cause EFMR, which also associates mental retardation and epilepsy exclusively in females.
Positive_regulation (cause) of EFMR associated with epilepsy, cognitive disorder and intellectual impairment
1) Confidence 0.69 Published 2009 Journal PLoS Genetics Section Body Doc Link PMC2633044 Disease Relevance 1.69 Pain Relevance 0

General Comments

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