INT251821

From wiki-pain
Jump to: navigation, search
Context Info
Confidence 0.42
First Reported 2008
Last Reported 2009
Negated 0
Speculated 0
Reported most in Body
Documents 3
Total Number 3
Disease Relevance 3.45
Pain Relevance 0.16

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

extracellular region (COL11A1) cell adhesion (COL11A1) protein binding, bridging (COL11A1)
extracellular matrix organization (COL11A1)
COL11A1 (Homo sapiens)
Pain Link Frequency Relevance Heat
backache 1 94.76 High High
Arthritis 4 67.84 Quite High
Osteoarthritis 11 66.80 Quite High
Pain 17 34.68 Quite Low
Inflammation 1 16.60 Low Low
imagery 2 5.00 Very Low Very Low Very Low
lumbar spondylosis 2 5.00 Very Low Very Low Very Low
Electroencephalography 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Deafness 6 100.00 Very High Very High Very High
Syndrome 117 98.52 Very High Very High Very High
Musculoskeletal Abnormalities 2 95.80 Very High Very High Very High
Low Back Pain 4 94.76 High High
Kyphosis 4 93.08 High High
Congenital Anomalies 8 90.12 High High
Scoliosis 4 88.60 High High
Paraplegia 1 85.20 High High
Sensorineural Hearing Loss 6 78.76 Quite High
Cleidocranial Dysplasia 11 69.68 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Variants of Stickler syndrome have been designated STL1 (vitreous type with mutations in COL2A1 gene), STL2 (early onset hearing loss and mutations in the COL 11A1 gene) and STL3 (non-ocular type caused by mutations in the COL11A2 gene).
Negative_regulation (loss) of COL 11A1 associated with deafness and syndrome
1) Confidence 0.42 Published 2008 Journal Cases J Section Body Doc Link PMC2579916 Disease Relevance 1.03 Pain Relevance 0
Variants of Stickler syndrome have been designated STL1 (vitreous type with mutations in COL2A1 gene), STL2 (early onset hearing loss and mutations in the COL 11A1 gene) and STL3 (non-ocular type caused by mutations in the COL11A2 gene).
Negative_regulation (loss) of COL 11A1 associated with deafness and syndrome
2) Confidence 0.42 Published 2009 Journal Pediatr Rheumatol Online J Section Body Doc Link PMC2645398 Disease Relevance 1.38 Pain Relevance 0.16
Variants of Stickler syndrome have been designated STL1 (vitreous type with mutations in COL2A1 gene), STL2 (early onset hearing loss and mutations in the COL 11A1 gene) and STL3 (non-ocular type caused by mutations in the COL11A2 gene).
Negative_regulation (loss) of STL2 associated with deafness and syndrome
3) Confidence 0.41 Published 2008 Journal Cases J Section Body Doc Link PMC2579916 Disease Relevance 1.04 Pain Relevance 0

General Comments

This test has worked.

Personal tools
Namespaces

Variants
Actions
Navigation
Toolbox