INT323051

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Context Info
Confidence 0.69
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.71
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.

CYP21A1P (Homo sapiens)
Pain Link Frequency Relevance Heat
dexamethasone 5 5.00 Very Low Very Low Very Low
iatrogenic 3 5.00 Very Low Very Low Very Low
agonist 2 5.00 Very Low Very Low Very Low
Pain 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Adrenal Cancer 137 85.76 High High
Reprotox - General 3 5 68.68 Quite High
Reprotox - General 1 8 68.16 Quite High
Hirsutism 16 5.00 Very Low Very Low Very Low
Polycystic Ovary Syndrome 14 5.00 Very Low Very Low Very Low
Alopecia 10 5.00 Very Low Very Low Very Low
Acne 7 5.00 Very Low Very Low Very Low
Precocious Puberty 4 5.00 Very Low Very Low Very Low
Stress 4 5.00 Very Low Very Low Very Low
Obesity 3 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Most of the mutations result from recombination between the active gene, CYP21A2, and its highly homologous non-functional pseudogene, CYP21A1P (i.e., gene conversion), which is located in close proximity within the HLA region on chromosome 6p21.3.
Localization (located) of CYP21A1P
1) Confidence 0.69 Published 2010 Journal International Journal of Pediatric Endocrinology Section Body Doc Link PMC2910408 Disease Relevance 0.71 Pain Relevance 0

General Comments

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