INT100589

Context Info Confidence 0.31 First Reported 2001 Last Reported 2001 Negated 0 Speculated 0 Reported most in Abstract Documents 1 Total Number 1 Disease Relevance 0.80 Pain Relevance 0.45

cytosol (FBXW11) nucleus (FBXW11) cell cycle (FBXW11) cytoplasm (FBXW11)

Anatomy Link Frequency HOS 1 FBXW11 (Homo sapiens)

Pain Link Frequency Relevance Heat Ultiva 2 94.84 anesthesia 4 94.08

Disease Link Frequency Relevance Heat Syndrome 4 100.00 Inborn Genetic Diseases 1 100.00 Heart Rate Under Development 1 87.60 Heart Disease 1 78.28 Aplasia 1 73.84 Abscess 1 72.72 Emergencies 1 71.00 Myocardial Infarction 1 5.00

Sentences Mentioned In

Key:

Protein

Mutation

Event

Anatomy

Negation

Speculation

Pain term

Disease term

HOS, a hereditary disease characterized by congenital malformations of the upper extremities and the heart, is often associated with rhythm disorders.

HOS Binding (associated) of in HOS associated with inborn genetic diseases and syndrome

1) Confidence 0.31 Published 2001 Journal Rev Esp Anestesiol Reanim Section Abstract Doc Link 11792287 Disease Relevance 0.80 Pain Relevance 0.45

General Comments

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