INT210279

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Context Info
Confidence 0.34
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.30
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 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Syndrome 46 99.80 Very High Very High Very High
Congenital Anomalies 7 5.00 Very Low Very Low Very Low
Heart Rate Under Development 5 5.00 Very Low Very Low Very Low
Charcot Marie Tooth Disease 4 5.00 Very Low Very Low Very Low
Chromosome Aberrations 4 5.00 Very Low Very Low Very Low
Neuropathic Pain 3 5.00 Very Low Very Low Very Low
Lissencephaly 2 5.00 Very Low Very Low Very Low
Hypertelorism 2 5.00 Very Low Very Low Very Low
Chromosome Deletion 2 5.00 Very Low Very Low Very Low
Muscle Hypotonia 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
This resulted in the insertion of the MDLS region into the middle SMS-REP/LCR17pB block, loss of the subtelomeric region 17p13.3, and part of 17p12, and duplication of the CMT1A and SMS regions.
Negative_regulation (loss) of Gene_expression (duplication) of CMT1A associated with syndrome
1) Confidence 0.34 Published 2007 Journal Hum Genet Section Body Doc Link PMC1914245 Disease Relevance 0.30 Pain Relevance 0

General Comments

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