INT228614

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Context Info
Confidence 0.58
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.86
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.

signal transduction (EXT1) transferase activity, transferring glycosyl groups (EXT1) Golgi apparatus (EXT1)
endoplasmic reticulum (EXT1)
Anatomy Link Frequency
cartilage 1
EXT1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 10 18.04 Low Low
imagery 2 5.00 Very Low Very Low Very Low
Spinal cord 1 5.00 Very Low Very Low Very Low
Arthritis 1 5.00 Very Low Very Low Very Low
medulla 1 5.00 Very Low Very Low Very Low
positron emission tomography 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Cancer 8 99.24 Very High Very High Very High
Osteochondroma 47 97.48 Very High Very High Very High
Multiple Hereditary Exostoses 45 96.64 Very High Very High Very High
Cleidocranial Dysplasia 3 92.68 High High
Chondrosarcoma 14 32.56 Quite Low
Pain 10 18.04 Low Low
Malignant Neoplastic Disease 16 9.20 Low Low
Congenital Anomalies 5 5.00 Very Low Very Low Very Low
Enchondromatosis 4 5.00 Very Low Very Low Very Low
Bone Cancer 3 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Loss of the remaining EXT1 wildtype allele has been demonstrated in the cartilage cap of osteochondromas from MO patients [39].
Negative_regulation (Loss) of EXT1 in cartilage associated with osteochondroma and multiple hereditary exostoses
1) Confidence 0.58 Published 2008 Journal Orphanet J Rare Dis Section Body Doc Link PMC2276198 Disease Relevance 0.86 Pain Relevance 0

General Comments

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