INT312968

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Context Info
Confidence 0.36
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.45
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.

mitochondrion (ACADVL) small molecule metabolic process (ACADVL)
ACADVL (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 6 5.00 Very Low Very Low Very Low
peripheral neuropathy 2 5.00 Very Low Very Low Very Low
halothane 2 5.00 Very Low Very Low Very Low
agonist 1 5.00 Very Low Very Low Very Low
Glutamate 1 5.00 Very Low Very Low Very Low
antiepileptic Drug 1 5.00 Very Low Very Low Very Low
backache 1 5.00 Very Low Very Low Very Low
positron emission tomography 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Disease 31 73.60 Quite High
Muscle Weakness 10 66.68 Quite High
Coronary Heart Disease 17 64.48 Quite High
Encephalopathy 4 63.04 Quite High
Hypoglycemia 10 62.40 Quite High
Congenital Anomalies 8 59.80 Quite High
Muscle Disease 23 5.00 Very Low Very Low Very Low
Glycogen Storage Disease 10 5.00 Very Low Very Low Very Low
Myoglobinuria 8 5.00 Very Low Very Low Very Low
Malignant Hyperthermia 8 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
As with VLCAD deficiency, there is a relationship between ETF/ETFDH genotype and phenotype in patients with MADD.In MADD early diagnosis is essential as some patients respond to pharmacological doses of riboflavin.
Gene_expression (deficiency) of VLCAD
1) Confidence 0.36 Published 2010 Journal Journal of Biomedicine and Biotechnology Section Body Doc Link PMC2877206 Disease Relevance 0.45 Pain Relevance 0

General Comments

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