INT312970

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Context Info
Confidence 0.01
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.56
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 (ACSL1) small molecule metabolic process (ACSL1) endoplasmic reticulum (ACSL1)
peroxisome (ACSL1) ligase activity (ACSL1)
Anatomy Link Frequency
urine 1
ACSL1 (Homo sapiens)
Pain Link Frequency Relevance Heat
peripheral neuropathy 2 11.52 Low Low
Pain 6 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 84.68 Quite High
Congenital Anomalies 8 78.28 Quite High
Hypoglycemia 10 61.52 Quite High
Coronary Heart Disease 17 60.32 Quite High
Encephalopathy 4 47.20 Quite Low
Muscle Weakness 10 45.92 Quite Low
Rhabdomyolysis 5 42.48 Quite Low
Liver Failure 1 36.16 Quite Low
Hypertrophic Cardiomyopathy 2 35.44 Quite Low
Myoglobinuria 8 13.56 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
In multiple acyl-CoA dehydrogenase deficiency (MADD, OMIM 231680) large excretion not only of glutaric acid but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids in urine occurs.
Negative_regulation (deficiency) of acyl-CoA in urine
1) Confidence 0.01 Published 2010 Journal Journal of Biomedicine and Biotechnology Section Body Doc Link PMC2877206 Disease Relevance 0.56 Pain Relevance 0

General Comments

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