INT307657

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Context Info
Confidence 0.67
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 0.53
Pain Relevance 0.17

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

cytosol (Mfn2) mitochondrion (Mfn2) GTPase activity (Mfn2)
Mfn2 (Rattus norvegicus)
Pain Link Frequency Relevance Heat
Action potential 12 65.04 Quite High
Demyelination 4 17.52 Low Low
Pain 4 5.00 Very Low Very Low Very Low
spinal stenosis 2 5.00 Very Low Very Low Very Low
Paresthesia 2 5.00 Very Low Very Low Very Low
Neuritis 2 5.00 Very Low Very Low Very Low
cva 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Hereditary Sensory And Autonomic Neuropathies 2 93.32 High High
Diabetic Nephropathy 2 93.08 High High
Ataxia 8 61.20 Quite High
Tremor 6 59.04 Quite High
Charcot Marie Tooth Disease 12 50.00 Quite Low
Demyelinating Disease 4 17.52 Low Low
Neuropathic Pain 20 5.00 Very Low Very Low Very Low
Muscle Weakness 10 5.00 Very Low Very Low Very Low
Peripheral Neuropathy 4 5.00 Very Low Very Low Very Low
Pain 4 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
These low frequencies of MFN2 mutations in CMT1 and dHMN made it unlikely for the International study to obtain MFN2 mutations in these CMT subtypes.
Gene_expression (mutations) of MFN2
1) Confidence 0.67 Published 2010 Journal BMC Med Genet Section Body Doc Link PMC2859816 Disease Relevance 0.30 Pain Relevance 0.08
We found the MFN2 mutation in 2 of 86 (2.3%) unrelated CMT1 families and in 1 of 15 (6.7%) unrelated dHMN families.
Gene_expression (mutation) of MFN2
2) Confidence 0.67 Published 2010 Journal BMC Med Genet Section Body Doc Link PMC2859816 Disease Relevance 0.24 Pain Relevance 0.09

General Comments

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