INT199159

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Context Info
Confidence 0.04
First Reported 2006
Last Reported 2006
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.42
Pain Relevance 0.03

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

endosome (RET) signal transduction (RET) plasma membrane (RET)
RET (Homo sapiens)
Pheo (Mus musculus)
Pain Link Frequency Relevance Heat
Glial derived neurotrophic factor 1 51.96 Quite High
imagery 4 5.00 Very Low Very Low Very Low
Catecholamine 4 5.00 Very Low Very Low Very Low
Dopamine 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
headache 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Multiple Endocrine Neoplasia Type 2a 61 100.00 Very High Very High Very High
Pheochromocytoma 24 100.00 Very High Very High Very High
Hypercalcemia 8 99.68 Very High Very High Very High
Thyroid Neoplasm 62 98.64 Very High Very High Very High
Syndrome 9 87.40 High High
Multiple Endocrine Neoplasia Type 2b 21 60.32 Quite High
Recurrence 1 33.36 Quite Low
Cancer 18 8.60 Low Low
Disease 5 5.00 Very Low Very Low Very Low
Metastasis 4 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Eighty-five percent of MEN2A patients have a codon 634 mutation, particularly C634R, strictly associated with the occurrence of PHEO and/or primary hyperparathyroidism [18].
MEN2A Binding (associated) of PHEO associated with multiple endocrine neoplasia type 2a, hypercalcemia and pheochromocytoma
1) Confidence 0.04 Published 2006 Journal Orphanet J Rare Dis Section Body Doc Link PMC1654141 Disease Relevance 1.42 Pain Relevance 0.03

General Comments

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