INT273150

Context Info Confidence 0.24 First Reported 2009 Last Reported 2009 Negated 0 Speculated 0 Reported most in Body Documents 1 Total Number 1 Disease Relevance 0.09 Pain Relevance 0

CHED1 (Homo sapiens)

Pain Link Frequency Relevance Heat Pain 5 5.00 Inflammation 3 5.00 fibrosis 2 5.00 peripheral neuropathy 1 5.00 imagery 1 5.00

Disease Link Frequency Relevance Heat Amyloidosis 3 92.44 Pressure And Volume Under Development 11 33.44 Syndrome 5 30.68 Deafness 1 29.92 Ocular Toxicity (including Many Sub-types) 3 27.72 Photophobia 6 20.12 Disease 25 5.00 Congenital Anomalies 21 5.00 Corneal Opacity 15 5.00 Corneal Disease 9 5.00

Sentences Mentioned In

Key:

Protein

Mutation

Event

Anatomy

Negation

Speculation

Pain term

Disease term

The gene responsible for CHED1 has been mapped to the pericentromeric region of chromosome 20 (20p11.2-q11.2) in an area overlapping a gene for one type of PPCD [147] and this distinct from the locus for CHED2 [116].

Regulation (responsible) of CHED1

1) Confidence 0.24 Published 2009 Journal Orphanet J Rare Dis Section Body Doc Link PMC2695576 Disease Relevance 0.09 Pain Relevance 0

General Comments

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