INT251831

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Context Info
Confidence 0.50
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.23
Pain Relevance 0.08

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

mitochondrion (C10orf2) cell death (C10orf2)
C10orf2 (Homo sapiens)
Pain Link Frequency Relevance Heat
peripheral neuropathy 2 93.56 High High
depression 2 62.84 Quite High
imagery 3 5.00 Very Low Very Low Very Low
anesthesia 1 5.00 Very Low Very Low Very Low
adenocard 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Peripheral Neuropathy 2 93.56 High High
Ataxia 3 92.48 High High
Voice Disorders 1 91.96 High High
Dysphagia 1 91.40 High High
Muscle Weakness 3 90.96 High High
Encephalopathy 1 78.20 Quite High
Chronic Progressive External Ophthalmoplegia 4 67.12 Quite High
Syndrome 3 65.12 Quite High
Tremor 2 65.04 Quite High
Foot Deformities 1 64.52 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Therefore, PEO1 mutations appear to be a common cause of family adPEO.
Positive_regulation (cause) of PEO1
1) Confidence 0.50 Published 2008 Journal Molecular Vision Section Body Doc Link PMC2579934 Disease Relevance 1.23 Pain Relevance 0.08

General Comments

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