INT273143

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Context Info
Confidence 0.01
First Reported 2009
Last Reported 2009
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 2
Disease Relevance 2.30
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 (Tat) biosynthetic process (Tat) cellular amino acid metabolic process (Tat)
Anatomy Link Frequency
skin 2
Tat (Mus musculus)
Pain Link Frequency Relevance Heat
Inflammation 6 29.72 Quite Low
Pain 10 5.00 Very Low Very Low Very Low
fibrosis 4 5.00 Very Low Very Low Very Low
peripheral neuropathy 2 5.00 Very Low Very Low Very Low
imagery 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Fabry Disease 4 100.00 Very High Very High Very High
Cystinosis 2 100.00 Very High Very High Very High
Lysosomal Storage Diseases 2 99.56 Very High Very High Very High
Mucopolysaccharidoses 14 98.44 Very High Very High Very High
Lipidosis 2 97.52 Very High Very High Very High
Sialidosis 4 97.08 Very High Very High Very High
Skin Diseases 2 95.96 Very High Very High Very High
Ichthyosis 4 95.00 High High
Darier's Disease 2 94.52 High High
Corneal Opacity 30 89.08 High High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Main differential diagnoses include various causes of monoclonal gammopathy, lecithin-cholesterol-acyltransferase deficiency, Fabry disease, cystinosis, tyrosine transaminase deficiency, systemic lysosomal storage diseases (mucopolysaccharidoses, lipidoses, mucolipidoses), and several skin diseases (X-linked ichthyosis, keratosis follicularis spinolosa decalvans).
Negative_regulation (deficiency) of tyrosine transaminase in skin associated with darier's disease, skin diseases, mucopolysaccharidoses, fabry disease, sialidosis, cystinosis, ichthyosis, lysosomal storage diseases and lipidosis
1) Confidence 0.01 Published 2009 Journal Orphanet J Rare Dis Section Abstract Doc Link PMC2695576 Disease Relevance 1.15 Pain Relevance 0
Main differential diagnoses include various causes of monoclonal gammopathy, lecithin-cholesterol-acyltransferase deficiency, Fabry disease, cystinosis, tyrosine transaminase deficiency, systemic lysosomal storage diseases (mucopolysaccharidoses, lipidoses, mucolipidoses), and several skin diseases (X-linked ichthyosis, keratosis follicularis spinolosa decalvans).
Negative_regulation (deficiency) of tyrosine transaminase in skin associated with darier's disease, skin diseases, mucopolysaccharidoses, fabry disease, sialidosis, cystinosis, ichthyosis, lysosomal storage diseases and lipidosis
2) Confidence 0.01 Published 2009 Journal Orphanet J Rare Dis Section Abstract Doc Link PMC2695576 Disease Relevance 1.15 Pain Relevance 0

General Comments

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