INT34699

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Context Info
Confidence 0.58
First Reported 1988
Last Reported 2004
Negated 0
Speculated 0
Reported most in Abstract
Documents 2
Total Number 2
Disease Relevance 0.83
Pain Relevance 0.27

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

mitochondrion (GCDH) small molecule metabolic process (GCDH) cellular nitrogen compound metabolic process (GCDH)
Anatomy Link Frequency
fibroblast 1
GCDH (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 2 90.24 High High
anesthesia 1 73.12 Quite High
Thalamus 1 57.52 Quite High
Disease Link Frequency Relevance Heat
Inborn Error Of Metabolism 1 99.84 Very High Very High Very High
Dystonia 6 93.92 High High
Syndrome 1 92.32 High High
Frailty 2 84.72 Quite High
Pain 1 73.04 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Glutaric aciduria type 1 is an inborn error of metabolism due to deficiency of glutaryl-CoA dehydrogenase.
Negative_regulation (deficiency) of glutaryl-CoA dehydrogenase associated with inborn error of metabolism
1) Confidence 0.58 Published 2004 Journal Stereotact Funct Neurosurg Section Abstract Doc Link 15305079 Disease Relevance 0.68 Pain Relevance 0.16
The diagnosis of glutaric aciduria type I (GAI) was confirmed by the absence of the enzyme glutaryl-CoA dehydrogenase in fibroblast culture.
Negative_regulation (absence) of glutaryl-CoA dehydrogenase in fibroblast
2) Confidence 0.42 Published 1988 Journal Dev Med Child Neurol Section Abstract Doc Link 3069526 Disease Relevance 0.15 Pain Relevance 0.10

General Comments

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