INT210275

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Context Info
Confidence 0.55
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 0.52
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 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Neuropathic Pain 6 99.16 Very High Very High Very High
Syndrome 92 98.72 Very High Very High Very High
Disease 4 82.88 Quite High
Chromosome Deletion 4 25.52 Quite Low
Chromosome Aberrations 8 19.84 Low Low
Congenital Anomalies 14 5.00 Very Low Very Low Very Low
Heart Rate Under Development 10 5.00 Very Low Very Low Very Low
Charcot Marie Tooth Disease 8 5.00 Very Low Very Low Very Low
Lissencephaly 4 5.00 Very Low Very Low Very Low
Hypertelorism 4 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Duplication of this gene causes CMT1A, a common inherited neuropathy characterized by myelin degeneration (Patel et al. 1992).
Positive_regulation (causes) of CMT1A associated with neuropathic pain
1) Confidence 0.55 Published 2007 Journal Hum Genet Section Body Doc Link PMC1914245 Disease Relevance 0.27 Pain Relevance 0
This resulted in the insertion of the MDLS region into the middle SMS-REP/LCR17pB block, loss of telomeric 17p and part of 17p12 and duplication of the CMT1A region.
Positive_regulation (duplication) of CMT1A associated with syndrome
2) Confidence 0.40 Published 2007 Journal Hum Genet Section Body Doc Link PMC1914245 Disease Relevance 0.25 Pain Relevance 0

General Comments

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