INT273144

From wiki-pain
Jump to: navigation, search
Context Info
Confidence 0.19
First Reported 2009
Last Reported 2009
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 3
Disease Relevance 1.70
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.

CHED1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 15 5.00 Very Low Very Low Very Low
Inflammation 9 5.00 Very Low Very Low Very Low
fibrosis 6 5.00 Very Low Very Low Very Low
peripheral neuropathy 3 5.00 Very Low Very Low Very Low
imagery 3 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Ocular Toxicity (including Many Sub-types) 9 99.92 Very High Very High Very High
Deafness 3 99.36 Very High Very High Very High
Syndrome 15 98.60 Very High Very High Very High
Photophobia 18 92.32 High High
Pressure And Volume Under Development 33 91.44 High High
Corneal Edema 18 79.60 Quite High
Disease 75 5.00 Very Low Very Low Very Low
Congenital Anomalies 63 5.00 Very Low Very Low Very Low
Corneal Opacity 45 5.00 Very Low Very Low Very Low
Corneal Disease 27 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
CHED2 is sometimes associated with receptive deafness (Harboyan syndrome) [142].
CHED2 Binding (associated) of associated with deafness and syndrome
1) Confidence 0.19 Published 2009 Journal Orphanet J Rare Dis Section Body Doc Link PMC2695576 Disease Relevance 0.64 Pain Relevance 0
Two types of CHED are recognized: CHED1 (autosomal dominant) and CHED2 (autosomal recessive) [140,141].
CHED1 Binding (recognized) of
2) Confidence 0.19 Published 2009 Journal Orphanet J Rare Dis Section Body Doc Link PMC2695576 Disease Relevance 0.53 Pain Relevance 0
Two types of CHED are recognized: CHED1 (autosomal dominant) and CHED2 (autosomal recessive) [140,141].
CHED Binding (recognized) of
3) Confidence 0.17 Published 2009 Journal Orphanet J Rare Dis Section Body Doc Link PMC2695576 Disease Relevance 0.53 Pain Relevance 0

General Comments

This test has worked.

Personal tools
Namespaces

Variants
Actions
Navigation
Toolbox