INT143836

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Context Info
Confidence 0.35
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Title
Documents 1
Total Number 1
Disease Relevance 0.92
Pain Relevance 0.09

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

nucleus (Foxc1) DNA binding (Foxc1) transcription factor binding (Foxc1)
cytoplasm (Foxc1)
Foxc1 (Mus musculus)
Pain Link Frequency Relevance Heat
Pain 1 86.16 High High
Disease Link Frequency Relevance Heat
Syndrome 3 99.00 Very High Very High Very High
Hydrocephalus 2 97.60 Very High Very High Very High
Deafness 2 97.04 Very High Very High Very High
Intellectual Impairment 1 89.92 High High
Growth Problems 1 88.96 High High
Arthralgia 1 86.40 High High
Eye Malformation 1 81.72 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld-Rieger anomaly, hydrocephaly, hearing loss): a 25-year follow up.
Negative_regulation (Absence) of FOXC1 associated with deafness, syndrome and hydrocephalus
1) Confidence 0.35 Published 2007 Journal Am. J. Med. Genet. A Section Title Doc Link 17486624 Disease Relevance 0.92 Pain Relevance 0.09

General Comments

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