INT352185

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Context Info
Confidence 0.01
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.83
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.

cell adhesion (PCDH11X) plasma membrane (PCDH11X)
Anatomy Link Frequency
embryo 1
PCDH11X (Homo sapiens)
Pain Link Frequency Relevance Heat
medulla 1 46.60 Quite Low
imagery 23 36.68 Quite Low
Pain 30 30.96 Quite Low
depression 8 5.00 Very Low Very Low Very Low
fibrosis 7 5.00 Very Low Very Low Very Low
cva 6 5.00 Very Low Very Low Very Low
Neuropathic pain 4 5.00 Very Low Very Low Very Low
aspirin 4 5.00 Very Low Very Low Very Low
rheumatoid arthritis 3 5.00 Very Low Very Low Very Low
Analgesic 3 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Fabry Disease 192 90.24 High High
Disease 47 87.60 High High
Reprotox - General 2 4 69.24 Quite High
Cyst 4 52.92 Quite High
Asymptomatic Diseases 2 49.84 Quite Low
Pain 35 30.96 Quite Low
Pressure Volume 2 Under Development 1 30.00 Quite Low
Angiokeratoma 4 27.52 Quite Low
Congenital Anomalies 15 25.36 Quite Low
Lymphedema 3 21.92 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
This phenotypic heterogeneity is thought to be partly due to lyonization [179], a process whereby one copy of the X-chromosome is randomly inactivated in all cells of the female embryo, so that heterozygous females are essentially a 'mosaic' of normal and mutant cells in varying proportions.
Negative_regulation (inactivated) of X-chromosome in embryo
1) Confidence 0.01 Published 2010 Journal Orphanet J Rare Dis Section Body Doc Link PMC3009617 Disease Relevance 0.83 Pain Relevance 0

General Comments

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