INT265823

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Context Info
Confidence 0.08
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.17
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.

methyltransferase activity (WHSC1) nucleolus (WHSC1) chromosome (WHSC1)
nucleus (WHSC1) DNA binding (WHSC1) cytoplasm (WHSC1)
WHSC1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Syndrome 4 100.00 Very High Very High Very High
Failure To Thrive 1 98.68 Very High Very High Very High
Intellectual Impairment 2 97.92 Very High Very High Very High
Convulsion 1 95.92 Very High Very High Very High
Cognitive Disorder 1 82.32 Quite High
Cleidocranial Dysplasia 31 81.80 Quite High
Mixed Connective Tissue Disorder 2 80.60 Quite High
Adhesions 1 76.40 Quite High
Disease 1 68.40 Quite High
Holoprosencephaly 2 56.12 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Chromosome region 4p16 has the critical genes that, when deleted, result in WHS (OMIM 194190), characterized by failure to thrive, mental retardation, distinct facial features, and seizures.
WHS Binding (result) of associated with convulsion, intellectual impairment, failure to thrive and syndrome
1) Confidence 0.08 Published 2008 Journal American Journal of Medical Genetics. Part a Section Body Doc Link PMC2663417 Disease Relevance 1.17 Pain Relevance 0

General Comments

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