INT205585

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Context Info
Confidence 0.45
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.70
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.

cell differentiation (Wnt4) Golgi apparatus (Wnt4) cell-cell signaling (Wnt4)
cytoplasm (Wnt4) anatomical structure development (Wnt4) extracellular space (Wnt4)
Wnt4 (Mus musculus)
Pain Link Frequency Relevance Heat
imagery 6 5.00 Very Low Very Low Very Low
fibrosis 2 5.00 Very Low Very Low Very Low
pain pelvic 1 5.00 Very Low Very Low Very Low
anesthesia 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Syndrome 65 97.72 Very High Very High Very High
Aplasia 29 90.60 High High
Hyperandrogenism 4 89.80 High High
Diabetes Mellitus 3 48.24 Quite Low
Polycystic Kidney Disease 1 44.88 Quite Low
Androgen Insensitivity 7 5.00 Very Low Very Low Very Low
Hearing Impairment 5 5.00 Very Low Very Low Very Low
Congenital Anomalies 5 5.00 Very Low Very Low Very Low
Infertility 5 5.00 Very Low Very Low Very Low
Reprotox - General 1 3 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Finally, the very recent report on a second patient bearing another WNT4 mutation has led to the conclusion that WNT4 deficiency is responsible for a clinical phenotype distinct from the classic MRKH syndrome [81].
Regulation (responsible) of WNT4 associated with syndrome
1) Confidence 0.45 Published 2007 Journal Orphanet J Rare Dis Section Body Doc Link PMC1832178 Disease Relevance 0.70 Pain Relevance 0

General Comments

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