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Context Info
Confidence 0.03
First Reported 1987
Last Reported 1987
Negated 0
Speculated 0
Reported most in Abstract
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 (Acadl) lipid metabolic process (Acadl) cytoplasm (Acadl)
Acadl (Rattus norvegicus)
Pain Link Frequency Relevance Heat
Pain 1 25.00 Low Low
Disease Link Frequency Relevance Heat
Disease 2 98.18 Very High Very High Very High
Coma 3 79.28 Quite High
Hypoglycemia 3 78.80 Quite High
Muscle Disease 1 73.60 Quite High
Coronary Heart Disease 1 71.76 Quite High
Fatty Liver 1 68.64 Quite High
Rhabdomyolysis 1 25.00 Low Low
Toxicity 1 25.00 Low Low
Hypertrophic Cardiomyopathy 1 25.00 Low Low
Muscle Weakness 1 25.00 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
There are now nine inherited diseases that have been identified in the pathway of mitochondrial fatty acid oxidation, including LCAD, MCAD, SCAD, and HMG-CoA lyase deficiencies, two forms each of CPT and MAD deficiencies and an incompletely characterized disorder of primary carnitine deficiency.
Negative_regulation (deficiencies) of LCAD associated with disease
1) Confidence 0.03 Published 1987 Journal Adv Pediatr Section Abstract Doc Link 3318304 Disease Relevance 0.56 Pain Relevance 0

General Comments

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