INT199647

Context Info Confidence 0.27 First Reported 2006 Last Reported 2006 Negated 0 Speculated 0 Reported most in Body Documents 1 Total Number 2 Disease Relevance 2.71 Pain Relevance 0

mitochondrion (Phyh) oxidoreductase activity (Phyh) peroxisome (Phyh)

Phyh (Mus musculus)

Pain Link Frequency Relevance Heat Bile 4 22.00 imagery 14 5.00 Sicca syndrome 12 5.00 Spinal cord 10 5.00 peripheral neuropathy 4 5.00 Action potential 4 5.00 medulla 4 5.00 palliative 2 5.00 cerebral cortex 2 5.00 midbrain 2 5.00

Disease Link Frequency Relevance Heat Refsum Disease 16 97.16 Rhizomelic Chondrodysplasia Punctata 6 94.88 Zellweger Syndrome 4 91.52 Peroxisomal Disorder 2 84.12 Skin Abnormalities 2 78.96 Deafness 8 76.96 Loss Of Sense Of Smell 2 76.56 Cerebellar Ataxia 96 75.44 Neuropathy 26 74.52 Retina Disease 6 73.56

Sentences Mentioned In

Key:

Protein

Mutation

Event

Anatomy

Negation

Speculation

Pain term

Disease term

The PHYH (or PAHX) gene placed on chromosome 10pter-p11.2 is responsible for the disorder in most of patients [40].

Regulation (responsible) of PAHX

1) Confidence 0.27 Published 2006 Journal Orphanet J Rare Dis Section Body Doc Link PMC1664553 Disease Relevance 1.35 Pain Relevance 0

The PHYH (or PAHX) gene placed on chromosome 10pter-p11.2 is responsible for the disorder in most of patients [40].

Regulation (responsible) of PHYH

2) Confidence 0.27 Published 2006 Journal Orphanet J Rare Dis Section Body Doc Link PMC1664553 Disease Relevance 1.36 Pain Relevance 0

General Comments

This test has worked.