INT129970

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Context Info
Confidence 0.41
First Reported 2005
Last Reported 2005
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 0.41
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.

small molecule metabolic process (GLA) extracellular region (GLA) Golgi apparatus (GLA)
lysosome (GLA) cytoplasm (GLA)
Anatomy Link Frequency
body 2
GLA (Homo sapiens)
Pain Link Frequency Relevance Heat
imagery 3 45.76 Quite Low
Pain 1 25.00 Low Low
Disease Link Frequency Relevance Heat
Lysosome Storage Disease 1 99.60 Very High Very High Very High
Fabry Disease 4 98.86 Very High Very High Very High
Disease 1 80.32 Quite High
Congenital Anomalies 4 25.00 Low Low
Pain 1 25.00 Low Low
Proteinuria 1 25.00 Low Low
Angiokeratoma 1 25.00 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Fabry disease is a rare X-linked lysosomal storage disorder caused by deficient activity of alpha-galactosidase A (alpha-Gal A) resulting in the storage of glycosphingolipids, especially globotriaosylceramide (Gb3), in cells throughout the body, causing life-threatening renal, cardiac, and cerebrovascular complications in hemizygous males and some heterozygous females.
Negative_regulation (deficient) of alpha-Gal A Binding (activity) of in body associated with fabry disease and lysosome storage disease
1) Confidence 0.41 Published 2005 Journal Medicine (Baltimore) Section Abstract Doc Link 16148726 Disease Relevance 0.41 Pain Relevance 0

General Comments

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