INT274268

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Context Info
Confidence 0.12
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.48
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.

Anatomy Link Frequency
optic 1
OPA2 (Homo sapiens)
Pain Link Frequency Relevance Heat
imagery 15 28.04 Quite Low
Neuritis 27 18.64 Low Low
Inflammation 17 5.00 Very Low Very Low Very Low
Multiple sclerosis 10 5.00 Very Low Very Low Very Low
cva 6 5.00 Very Low Very Low Very Low
Pain 5 5.00 Very Low Very Low Very Low
alcohol 3 5.00 Very Low Very Low Very Low
Demyelination 3 5.00 Very Low Very Low Very Low
Spinal cord 2 5.00 Very Low Very Low Very Low
methotrexate 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Optic Atrophy 2 98.82 Very High Very High Very High
Optic Disorders 85 98.32 Very High Very High Very High
Oxidative Phosphorylation Disease 1 95.68 Very High Very High Very High
Deafness 1 94.96 High High
Diabetes Mellitus 4 94.04 High High
Marinesco Sjogren Syndrome 1 92.96 High High
Ataxia 4 89.52 High High
Frailty 1 86.72 High High
Pallor 8 81.16 Quite High
Scotoma 10 70.68 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
An X-linked optic atrophy has also been described and the genetic mutation has been localized to Xp11.4–Xp11.2 (OPA2) (Katz et al 2006).
Localization (localized) of OPA2 in optic associated with optic atrophy
1) Confidence 0.12 Published 2007 Journal Clinical ophthalmology (Auckland, N.Z.) Section Body Doc Link PMC2701125 Disease Relevance 1.48 Pain Relevance 0

General Comments

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