Gene table: search width pubmed_id = 8816708


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

protein
All allelic disease phenotypes - locus/disease symbols
Neuropathy, congenital hypomyelinating, 2 - ( AR)
14.35
8816708
MPZ (1q22)
Myelin protein zero
* Charcot-Marie-Tooth disease, type 2I - CMT2I
* Charcot-Marie-Tooth disease, type 2J - CMT2J
* Charcot-Marie-Tooth disease, type 1B - CMT1B
* Neuropathy, congenital hypomyelinating, 2 - CHN2
* Charcot-Marie-Tooth disease, dominant intermediate D - CMTDID
* Dejerine-Sottas syndrome - DSSA