INT123640

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Context Info
Confidence 0.01
First Reported 2005
Last Reported 2007
Negated 1
Speculated 0
Reported most in Abstract
Documents 2
Total Number 2
Disease Relevance 0.87
Pain Relevance 0.06

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

LGMD1H (Homo sapiens)
Pain Link Frequency Relevance Heat
anesthesia 1 55.44 Quite High
Pain 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Muscular Dystrophy 17 99.96 Very High Very High Very High
Limb-girdle Muscular Dystrophies 7 97.36 Very High Very High Very High
Hypertrophy 2 60.48 Quite High
Autolysis 1 34.88 Quite Low
Muscular Atrophy 3 5.00 Very Low Very Low Very Low
Disease 2 5.00 Very Low Very Low Very Low
Contracture 2 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
Abnormal Reflex 1 5.00 Very Low Very Low Very Low
Congenital Anomalies 1 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
To date, at least seven different forms of autosomal dominantly-inherited LGMD (LGMD1) have been recognized, and 11 in cases of autosomal recessively-inherited ones (LGMD2).
LGMD1 Binding (recognized) of associated with muscular dystrophy
1) Confidence 0.01 Published 2007 Journal Journal of Korean Medical Science Section Body Doc Link PMC2693639 Disease Relevance 0.28 Pain Relevance 0
A genomewide scan was undertaken in five families who did not show linkage to the LGMD2H locus on chromosome 9.
LGMD2H Neg (not) Binding (linkage) of
2) Confidence 0.00 Published 2005 Journal Hum. Mutat. Section Abstract Doc Link 15580560 Disease Relevance 0.58 Pain Relevance 0.06

General Comments

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