Gene table: search width pubmed_id = 8012388


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Hereditary Neuropathy with Liability to Pressure Palsies - (AD)
14.6
8012388
8112739
8422677
PMP22 (17p12-p11.2)
Peripheral myelin protein 22
* Neuropathy, recurrent, with pressure palsies - HNPP
* Dejerine-Sottas Syndrome - DSSB
* Charcot-Marie-Tooth disease, type 1A - CMT1A
* Charcot-Marie-Tooth disease, type 1E - CMT1E