INT308322

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Context Info
Confidence 0.25
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.84
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.

ATP6 (Homo sapiens)
Pain Link Frequency Relevance Heat
peripheral neuropathy 1 5.00 Very Low Very Low Very Low
Glutamate 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
imagery 1 5.00 Very Low Very Low Very Low
alcohol 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Leber Hereditary Optic Atrophy 71 99.00 Very High Very High Very High
Leigh Syndrome 2 90.92 High High
Glaucoma 11 90.08 High High
Disease 7 84.88 Quite High
Neuropathic Pain 1 80.56 Quite High
Ataxia 1 79.60 Quite High
Retina Disease 1 78.96 Quite High
Optic Disorders 8 48.72 Quite Low
Stress 15 35.88 Quite Low
Mitochondrial Myopathies 1 33.28 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Two nonsynonymous changes in ATPase6 (p.T53I and p.W48R) were also identified, one of which (p.W48R) was pathogenic and present in one patient (LHON 5).
Regulation (changes) of ATPase6 associated with leber hereditary optic atrophy
1) Confidence 0.25 Published 2010 Journal Molecular Vision Section Body Doc Link PMC2862244 Disease Relevance 1.84 Pain Relevance 0

General Comments

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