INT199647

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Context Info
Confidence 0.27
First Reported 2006
Last Reported 2006
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 2.71
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.

mitochondrion (Phyh) oxidoreductase activity (Phyh) peroxisome (Phyh)
Phyh (Mus musculus)
Pain Link Frequency Relevance Heat
Bile 4 22.00 Low Low
imagery 14 5.00 Very Low Very Low Very Low
Sicca syndrome 12 5.00 Very Low Very Low Very Low
Spinal cord 10 5.00 Very Low Very Low Very Low
peripheral neuropathy 4 5.00 Very Low Very Low Very Low
Action potential 4 5.00 Very Low Very Low Very Low
medulla 4 5.00 Very Low Very Low Very Low
palliative 2 5.00 Very Low Very Low Very Low
cerebral cortex 2 5.00 Very Low Very Low Very Low
midbrain 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Refsum Disease 16 97.16 Very High Very High Very High
Rhizomelic Chondrodysplasia Punctata 6 94.88 High High
Zellweger Syndrome 4 91.52 High High
Peroxisomal Disorder 2 84.12 Quite High
Skin Abnormalities 2 78.96 Quite High
Deafness 8 76.96 Quite High
Loss Of Sense Of Smell 2 76.56 Quite High
Cerebellar Ataxia 96 75.44 Quite High
Neuropathy 26 74.52 Quite High
Retina Disease 6 73.56 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The PHYH (or PAHX) gene placed on chromosome 10pter-p11.2 is responsible for the disorder in most of patients [40].
Regulation (responsible) of PAHX
1) Confidence 0.27 Published 2006 Journal Orphanet J Rare Dis Section Body Doc Link PMC1664553 Disease Relevance 1.35 Pain Relevance 0
The PHYH (or PAHX) gene placed on chromosome 10pter-p11.2 is responsible for the disorder in most of patients [40].
Regulation (responsible) of PHYH
2) Confidence 0.27 Published 2006 Journal Orphanet J Rare Dis Section Body Doc Link PMC1664553 Disease Relevance 1.36 Pain Relevance 0

General Comments

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