INT166835

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Context Info
Confidence 0.02
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 1.08
Pain Relevance 0.08

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

cytosol (HBB) transport (HBB)
HBB (Homo sapiens)
Pain Link Frequency Relevance Heat
abdominal pain 2 76.48 Quite High
Bile 2 45.04 Quite Low
Pain 1 25.00 Low Low
Disease Link Frequency Relevance Heat
Sickle Cell Anemia 6 99.44 Very High Very High Very High
Hemolytic Anemia 1 95.80 Very High Very High Very High
Frailty 1 80.56 Quite High
Liver Disease 3 79.36 Quite High
Abdominal Pain 2 76.48 Quite High
Infarction 1 71.84 Quite High
Hemosiderosis 2 65.76 Quite High
Hepatitis 1 64.32 Quite High
Gallstones 1 54.48 Quite High
Hyperbilirubinemia 2 40.96 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Sickle cell disease (SCD) is an autosomal recessive abnormality of the beta-globin chain of hemoglobin (Hb), resulting in poorly deformable sickled cells that cause microvascular occlusion and hemolytic anemia.
Regulation (abnormality) of beta-globin chain associated with sickle cell anemia and hemolytic anemia
1) Confidence 0.02 Published 2010 Journal Clin. Gastroenterol. Hepatol. Section Abstract Doc Link 20215064 Disease Relevance 1.08 Pain Relevance 0.08

General Comments

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