INT272204

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Context Info
Confidence 0.06
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Title
Documents 1
Total Number 1
Disease Relevance 0.57
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.

extracellular space (FKTN) Golgi apparatus (FKTN) endoplasmic reticulum (FKTN)
nucleus (FKTN)
Anatomy Link Frequency
limb 1
FKTN (Homo sapiens)
Pain Link Frequency Relevance Heat
Pain 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Muscular Dystrophy 17 100.00 Very High Very High Very High
Disease 2 98.52 Very High Very High Very High
Muscular Atrophy 3 5.00 Very Low Very Low Very Low
Contracture 2 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
Abnormal Reflex 1 5.00 Very Low Very Low Very Low
Limb-girdle Muscular Dystrophies 1 5.00 Very Low Very Low Very Low
Congenital Anomalies 1 5.00 Very Low Very Low Very Low
Hypertrophy 1 5.00 Very Low Very Low Very Low
Intellectual Impairment 1 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Mutations of CAPN3 in Korean Patients with Limb-Girdle Muscular Dystrophy

The limb-girdle muscular dystrophy type 2A (LGMD2A) is a recessively inherited disease caused by a mutation of the calpain 3 gene (CAPN3), and is considered one of the most prevalent subtypes of limb-girdle muscular dystrophy (LGMD).

Positive_regulation (girdle) of muscular dystrophy type 2A in limb associated with muscular dystrophy and disease
1) Confidence 0.06 Published 2007 Journal Journal of Korean Medical Science Section Title Doc Link PMC2693639 Disease Relevance 0.57 Pain Relevance 0

General Comments

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