INT175898

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Context Info
Confidence 0.50
First Reported 2004
Last Reported 2004
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 1.24
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.

plasma membrane (PKD1) nucleus (PKD1) cilium (PKD1)
cytoplasm (PKD1)
PKD1 (Homo sapiens)
Pain Link Frequency Relevance Heat
headache 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Disease 32 100.00 Very High Very High Very High
Cerebral Aneurysm 8 97.12 Very High Very High Very High
Cyst 6 94.60 High High
Chronic Renal Failure 18 93.88 High High
Autosomal Dominant Polycystic Kidney 42 80.80 Quite High
Polycystic Kidney Disease 12 34.40 Quite Low
Hypertension 4 5.00 Very Low Very Low Very Low
Helminth Infection 2 5.00 Very Low Very Low Very Low
Coronary Artery Disease 2 5.00 Very Low Very Low Very Low
Cervical Cancer 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
PKD1 mutations occur throughout the gene with apparently no mutational "hot-spots", rendering characterization of all disease causing PKD1 mutations in various ethnic groups essential for comprehension of molecular mechanism of the disease and for providing diagnostic genetic testing.
Positive_regulation (causing) of PKD1 associated with disease
1) Confidence 0.50 Published 2004 Journal BMC Med Genet Section Body Doc Link PMC356914 Disease Relevance 0.25 Pain Relevance 0
Two known genes are responsible for this disease: PKD1 (MIM# 601313) at 16p13.3 [3-6] and PKD2 (MIM# 173910) at 4q21-23 [7].
Positive_regulation (responsible) of PKD1 associated with disease
2) Confidence 0.46 Published 2004 Journal BMC Med Genet Section Body Doc Link PMC356914 Disease Relevance 0.98 Pain Relevance 0

General Comments

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