INT320805

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Context Info
Confidence 0.57
First Reported 2010
Last Reported 2010
Negated 0
Speculated 1
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 1.10
Pain Relevance 0.19

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 (SLC26A2) transmembrane transport (SLC26A2)
Anatomy Link Frequency
pectus 1
rMED 1
SLC26A2 (Homo sapiens)
Pain Link Frequency Relevance Heat
Osteoarthritis 12 83.84 Quite High
Pain 36 68.20 Quite High
backache 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Congenital Anomalies 8 99.28 Very High Very High Very High
Scoliosis 10 89.72 High High
Osteoarthritis 12 84.64 Quite High
Contracture 16 75.52 Quite High
Dislocations 48 72.40 Quite High
Pain 26 68.20 Quite High
Osteochondrodysplasias 38 50.00 Quite Low
Arthralgia 6 48.00 Quite Low
Foot Deformities 2 45.04 Quite Low
Disease 6 42.64 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
A genomic DNA sample was analysed for DTDST mutation because of clinical and radiographic signs similar to reported cases of rMED [9,10].
Spec (analysed) Gene_expression (mutation) of DTDST in rMED
1) Confidence 0.57 Published 2010 Journal BMC Musculoskelet Disord Section Body Doc Link PMC2902411 Disease Relevance 0.19 Pain Relevance 0.04
As a pectus carinatum was also known in our patient's brother, who had no further skeletal abnormalities, it was probably not caused by the DTDST mutation.
Gene_expression (mutation) of DTDST in pectus associated with congenital anomalies
2) Confidence 0.57 Published 2010 Journal BMC Musculoskelet Disord Section Body Doc Link PMC2902411 Disease Relevance 0.91 Pain Relevance 0.15

General Comments

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