INT332543

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Context Info
Confidence 0.04
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.81
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.

transport (Atp2b2) cell morphogenesis (Atp2b2) endoplasmic reticulum (Atp2b2)
cilium (Atp2b2) transmembrane transport (Atp2b2) cytoplasm (Atp2b2)
Atp2b2 (Mus musculus)
Pain Link Frequency Relevance Heat
fibrosis 7 49.76 Quite Low
Arthritis 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
antagonist 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Syndrome 48 100.00 Very High Very High Very High
Ectopia Lentis 2 100.00 Very High Very High Very High
Cleidocranial Dysplasia 32 92.48 High High
Glaucoma 1 90.64 High High
Dislocations 1 88.28 High High
Targeted Disruption 1 67.04 Quite High
Tracheal Stenosis 1 61.08 Quite High
Facies 2 57.76 Quite High
Growth Problems 3 56.84 Quite High
Contracture 4 52.60 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The recent discovery of ADAMTS17 and ADAMTSL4 mutations in a WMS-like syndrome [24] and in recessive isolated ectopia lentis [25] respectively, further strengthen genetic associations between fibrillin-1 microfibrils and the ADAMTS superfamily.
Gene_expression (microfibrils) of WMS associated with ectopia lentis and syndrome
1) Confidence 0.04 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2941456 Disease Relevance 1.81 Pain Relevance 0

General Comments

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