INT120176

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Context Info
Confidence 0.15
First Reported 2004
Last Reported 2008
Negated 0
Speculated 0
Reported most in Abstract
Documents 2
Total Number 2
Disease Relevance 0.79
Pain Relevance 0.20

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

cytosol (HK1) mitochondrion (HK1) small molecule metabolic process (HK1)
nucleolus (HK1) nucleus (HK1) carbohydrate metabolic process (HK1)
Anatomy Link Frequency
muscle 2
HK1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 2 97.84 Very High Very High Very High
Disease Link Frequency Relevance Heat
Glycogen Storage Disease 4 98.94 Very High Very High Very High
Disease 4 98.42 Very High Very High Very High
Pain 2 97.68 Very High Very High Very High
Myoglobinuria 3 5.00 Very Low Very Low Very Low
Fatigue 2 5.00 Very Low Very Low Very Low
Acute Renal Failure 2 5.00 Very Low Very Low Very Low
Cramps 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
BACKGROUND: McArdle's disease (Glycogen Storage Disease type V) is caused by the absence of the glycolytic enzyme, muscle phosphorylase.
Phosphorylation (phosphorylase) of glycolytic enzyme in muscle associated with glycogen storage disease and disease
1) Confidence 0.15 Published 2004 Journal Cochrane Database Syst Rev Section Abstract Doc Link 15266486 Disease Relevance 0.45 Pain Relevance 0.10
BACKGROUND: McArdle disease (Glycogen Storage Disease type V) is caused by the absence of the glycolytic enzyme, muscle phosphorylase.
Phosphorylation (phosphorylase) of glycolytic enzyme in muscle associated with glycogen storage disease and disease
2) Confidence 0.06 Published 2008 Journal Cochrane Database Syst Rev Section Abstract Doc Link 18425888 Disease Relevance 0.35 Pain Relevance 0.10

General Comments

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