INT229793

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Context Info
Confidence 0.43
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.49
Pain Relevance 1.17

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

small molecule metabolic process (SPTLC1) endoplasmic reticulum (SPTLC1) biosynthetic process (SPTLC1)
transferase activity, transferring acyl groups (SPTLC1)
SPTLC1 (Homo sapiens)
Pain Link Frequency Relevance Heat
Hsan 94 97.48 Very High Very High Very High
imagery 2 86.68 High High
Pain 4 21.28 Low Low
unmyelinated 2 5.00 Very Low Very Low Very Low
Spinal cord 1 5.00 Very Low Very Low Very Low
lancinating pain 1 5.00 Very Low Very Low Very Low
syringomyelia 1 5.00 Very Low Very Low Very Low
Demyelination 1 5.00 Very Low Very Low Very Low
diabetic neuropathy 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Hereditary Sensory And Autonomic Neuropathies 101 97.48 Very High Very High Very High
Necrosis 5 88.48 High High
Infection 6 88.00 High High
Neuropathic Pain 13 77.68 Quite High
Disease 24 56.16 Quite High
Frailty 1 54.00 Quite High
Pain 5 21.28 Low Low
Hypohidrosis 1 20.56 Low Low
Syndrome 7 5.00 Very Low Very Low Very Low
Charcot Marie Tooth Disease 6 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Large families in which mutations in SPTLC1 and RAB7 are excluded can be used for genome wide linkage studies to detect a novel HSN I locus or to confirm linkage to the third known HSN I locus (i.e. the HSN IB locus).
Negative_regulation (excluded) of Positive_regulation (mutations) of SPTLC1 associated with hsan
1) Confidence 0.43 Published 2008 Journal Orphanet J Rare Dis Section Body Doc Link PMC2311280 Disease Relevance 1.49 Pain Relevance 1.17

General Comments

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