INT81553

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Context Info
Confidence 0.03
First Reported 1999
Last Reported 2001
Negated 0
Speculated 0
Reported most in Abstract
Documents 2
Total Number 2
Disease Relevance 2.13
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.

cell differentiation (PMP22) plasma membrane (PMP22)
PMP22 (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 2 25.00 Low Low
Disease Link Frequency Relevance Heat
Neuropathy 18 95.72 Very High Very High Very High
Demyelinating Disease 8 95.04 Very High Very High Very High
Charcot Marie Tooth Disease 12 91.32 High High
Disease 5 90.72 High High
Syndrome 4 34.64 Quite Low
Paralysis 8 25.00 Low Low
Brachial Plexus Neuritis 2 25.00 Low Low
Brachial Plexus Neuropathies 2 25.00 Low Low
Peripheral Neuropathy 2 25.00 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
CMT1A is most often associated with a tandem 1.5-megabase (Mb) duplication in chromosome 17p11.2-12, or in rare patients may result from a point mutation in the peripheral myelin protein-22 (PMP22) gene.
CMT1A Binding (associated) of
1) Confidence 0.03 Published 1999 Journal Brain Pathol. Section Abstract Doc Link 10219749 Disease Relevance 1.10 Pain Relevance 0
CMT1A is most often associated with a tandem 1.5-megabase (Mb) duplication in chromosome 17p11.2-12, or in rare patients may result from a point mutation in the peripheral myelin protein-22 (PMP22) gene.
CMT1A Binding (associated) of
2) Confidence 0.03 Published 2001 Journal Phys Med Rehabil Clin N Am Section Abstract Doc Link 11345007 Disease Relevance 1.03 Pain Relevance 0

General Comments

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