INT330759

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Context Info
Confidence 0.04
First Reported 2010
Last Reported 2010
Negated 1
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.39
Pain Relevance 0.35

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

mitochondrion (LETMD1)
LETMD1 (Homo sapiens)
Pain Link Frequency Relevance Heat
fibrosis 14 100.00 Very High Very High Very High
abdominal pain 7 69.08 Quite High
Bile 3 16.00 Low Low
Inflammation 3 5.00 Very Low Very Low Very Low
imagery 2 5.00 Very Low Very Low Very Low
Chronic pancreatitis 1 5.00 Very Low Very Low Very Low
Inflammatory response 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Cystic Fibrosis 14 100.00 Very High Very High Very High
Exocrine Pancreatic Insufficiency 9 98.44 Very High Very High Very High
Failure To Thrive 1 90.92 High High
Sepsis 2 86.28 High High
Bronchiectasis 1 78.72 Quite High
Ileus 1 74.80 Quite High
Abdominal Pain 7 69.08 Quite High
Recurrence 1 68.64 Quite High
Appetite Loss 1 65.68 Quite High
Weight Loss 1 64.64 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
G542X is a Class I mutation that results in the complete failure to synthesize functional cystic fibrosis transmembrane conductance regulator (CFTR) and is usually associated with pancreatic insufficiency.
Neg (failure) Gene_expression (synthesize) of regulator associated with fibrosis, exocrine pancreatic insufficiency and cystic fibrosis
1) Confidence 0.04 Published 2010 Journal J Med Case Reports Section Body Doc Link PMC2936924 Disease Relevance 1.39 Pain Relevance 0.35

General Comments

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