INT223092

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Context Info
Confidence 0.01
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.72
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.

protein transporter activity (AP2S1) cytosol (AP2S1) transport (AP2S1)
vesicle-mediated transport (AP2S1) plasma membrane (AP2S1)
AP2S1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Antihistamine 4 5.00 Very Low Very Low Very Low
imagery 3 5.00 Very Low Very Low Very Low
palliative 2 5.00 Very Low Very Low Very Low
carpal tunnel syndrome 2 5.00 Very Low Very Low Very Low
Pain 2 5.00 Very Low Very Low Very Low
corticosteroid 1 5.00 Very Low Very Low Very Low
Spinal cord 1 5.00 Very Low Very Low Very Low
Central nervous system 1 5.00 Very Low Very Low Very Low
Peripheral nervous system 1 5.00 Very Low Very Low Very Low
anticonvulsant 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Disease 43 99.78 Very High Very High Very High
Mucopolysaccharidosis Ii 7 98.82 Very High Very High Very High
Lysosome Storage Disease 8 98.12 Very High Very High Very High
Syndrome 2 53.68 Quite High
Airway Obstruction 6 40.88 Quite Low
Macroglossia 1 38.80 Quite Low
Tracheomalacia 2 35.44 Quite Low
Apnoea 3 30.24 Quite Low
Coronary Heart Disease 3 9.44 Low Low
Cleidocranial Dysplasia 5 7.04 Low Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
First described by Major Charles Hunter in 1917 [15], mucopolysaccharidosis type II (MPS II or Hunter syndrome; OMIM +309900) is an X-linked recessive disease caused by deficiency of the lysosomal enzyme iduronate-2-sulphatase (I2S).
Negative_regulation (deficiency) of I2S associated with mucopolysaccharidosis ii, disease and lysosome storage disease
1) Confidence 0.01 Published 2007 Journal Eur J Pediatr Section Body Doc Link PMC2234442 Disease Relevance 0.72 Pain Relevance 0

General Comments

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