INT170885

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Context Info
Confidence 0.01
First Reported 2001
Last Reported 2001
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.40
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.

peptidase activity (PRSS1) extracellular space (PRSS1) extracellular region (PRSS1)
PRSS1 (Homo sapiens)
RHBDD2 (Homo sapiens)
RHBDD2 - R122H (1)
Pain Link Frequency Relevance Heat
Chronic pancreatitis 4 43.20 Quite Low
fibrosis 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Pancreatitis 13 98.04 Very High Very High Very High
Autolysis 12 92.72 High High
Iron Overload 1 5.00 Very Low Very Low Very Low
Cystic Fibrosis 1 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Disruption of this site by a missense mutation – R122H (originally termed R117H in the chymotrypsin numbering system [2]; for a discussion of mutation nomenclature see [3,4]) – in the human cationic trypsinogen (PRSS1; OMIM 276000) has been associated with most of the large kindreds with hereditary pancreatitis (HP; OMIM 167800) [1].
PRSS1 Binding (associated) of R122H (R122H) associated with pancreatitis
1) Confidence 0.01 Published 2001 Journal BMC Genet Section Body Doc Link PMC60523 Disease Relevance 0.40 Pain Relevance 0

General Comments

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