INT143339

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Context Info
Confidence 0.13
First Reported 2007
Last Reported 2010
Negated 0
Speculated 0
Reported most in Abstract
Documents 2
Total Number 2
Disease Relevance 1.24
Pain Relevance 0.42

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

cytoplasm (CCM2)
CCM2 (Homo sapiens)
Pain Link Frequency Relevance Heat
headache 2 89.96 High High
cva 2 88.20 High High
Central nervous system 2 82.88 Quite High
Migraine 1 70.36 Quite High
Spinal cord 1 64.56 Quite High
Disease Link Frequency Relevance Heat
Hemangioma 7 93.68 High High
Headache 3 89.96 High High
Hemorrhage 1 88.20 High High
Epilepsy 1 87.68 High High
Vascular Malformations 2 80.96 Quite High
Cv General 3 Under Development 1 68.64 Quite High
Convulsion 1 67.12 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The CCM genes are identified as Krit 1 (CCM1), MGC4607 (CCM2), and PDCD10 (CCM3).
Gene_expression (identified) of MGC4607
1) Confidence 0.13 Published 2010 Journal Neurosurg Rev Section Abstract Doc Link 19760287 Disease Relevance 0.35 Pain Relevance 0.21
In a CCM2 affected family, we also report a novel causative mutation, (54_55delAC) in exon 2 of the MGC4607 gene, that produces a truncated protein containing only 22 amino acids.
Gene_expression (produces) of MGC4607 gene
2) Confidence 0.02 Published 2007 Journal Am. J. Med. Genet. B Neuropsychiatr. Genet. Section Abstract Doc Link 17440989 Disease Relevance 0.89 Pain Relevance 0.21

General Comments

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