INT308301

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Context Info
Confidence 0.08
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.27
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.

nucleolus (Hnf1b) nucleus (Hnf1b) embryo development (Hnf1b)
DNA binding (Hnf1b)
Hnf1b (Rattus norvegicus)
Pain Link Frequency Relevance Heat
imagery 2 5.00 Very Low Very Low Very Low
pain pelvic 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Syndrome 18 90.64 High High
Aplasia 3 58.60 Quite High
Rheumatoid Arthritis 12 43.24 Quite Low
Congenital Anomalies 6 43.08 Quite Low
Cleidocranial Dysplasia 13 19.92 Low Low
Reprotox - General 1 2 5.00 Very Low Very Low Very Low
Death 1 5.00 Very Low Very Low Very Low
Emergencies 1 5.00 Very Low Very Low Very Low
Hiatal Hernia 1 5.00 Very Low Very Low Very Low
Vomiting 1 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The other 20 MRKH patients in this study, as in our case, do not carry the microdeletion and sequencing of TCF2 and LHX1 genes does not detect pathological mutations.
Gene_expression (microdeletion) of TCF2
1) Confidence 0.08 Published 2010 Journal Orphanet J Rare Dis Section Body Doc Link PMC2862022 Disease Relevance 0.27 Pain Relevance 0

General Comments

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