INT312968

Context Info Confidence 0.36 First Reported 2010 Last Reported 2010 Negated 0 Speculated 0 Reported most in Body Documents 1 Total Number 1 Disease Relevance 0.45 Pain Relevance 0

mitochondrion (ACADVL) small molecule metabolic process (ACADVL)

ACADVL (Homo sapiens)

Pain Link Frequency Relevance Heat Pain 6 5.00 peripheral neuropathy 2 5.00 halothane 2 5.00 agonist 1 5.00 Glutamate 1 5.00 antiepileptic Drug 1 5.00 backache 1 5.00 positron emission tomography 1 5.00

Disease Link Frequency Relevance Heat Disease 31 73.60 Muscle Weakness 10 66.68 Coronary Heart Disease 17 64.48 Encephalopathy 4 63.04 Hypoglycemia 10 62.40 Congenital Anomalies 8 59.80 Muscle Disease 23 5.00 Glycogen Storage Disease 10 5.00 Myoglobinuria 8 5.00 Malignant Hyperthermia 8 5.00

Sentences Mentioned In

Key:

Protein

Mutation

Event

Anatomy

Negation

Speculation

Pain term

Disease term

As with VLCAD deficiency, there is a relationship between ETF/ETFDH genotype and phenotype in patients with MADD.In MADD early diagnosis is essential as some patients respond to pharmacological doses of riboflavin.

Gene_expression (deficiency) of VLCAD

1) Confidence 0.36 Published 2010 Journal Journal of Biomedicine and Biotechnology Section Body Doc Link PMC2877206 Disease Relevance 0.45 Pain Relevance 0

General Comments

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