INT157213

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Context Info
Confidence 0.30
First Reported 2009
Last Reported 2009
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 0.68
Pain Relevance 0.22

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

mitochondrion (AGXT) small molecule metabolic process (AGXT) plasma membrane (SGCG)
cytoskeleton (SGCG) peroxisome (AGXT) cytoskeleton organization (SGCG)
Anatomy Link Frequency
peripheral nervous system 1
AGXT (Homo sapiens)
SGCG (Homo sapiens)
Pain Link Frequency Relevance Heat
Peripheral nervous system 1 100.00 Very High Very High Very High
Hsan 2 99.98 Very High Very High Very High
Disease Link Frequency Relevance Heat
Hereditary Sensory And Autonomic Neuropathies 8 100.00 Very High Very High Very High
Neurodegenerative Disease 1 100.00 Very High Very High Very High
Disease 1 75.00 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Hereditary sensory neuropathy type 1 (HSAN I) is an autosomal dominant inherited neurodegenerative disorder of the peripheral nervous system associated with mutations in the SPTLC1 subunit of the serine palmitoyltransferase (SPT).
SPT Binding (associated) of type in peripheral nervous system associated with peripheral nervous system, neurodegenerative disease, hereditary sensory and autonomic neuropathies and hsan
1) Confidence 0.30 Published 2009 Journal Neurogenetics Section Abstract Doc Link 19132419 Disease Relevance 0.68 Pain Relevance 0.22

General Comments

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