Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
CUI: C0030554
Disease: Paresthesia
Paresthesia 		0.410 AlteredExpression BEFREE On the other end of the spectrum, CMT1A leads to a more uniform demyelination and axonal loss, resulting in severe progressive distal weakness and paresthesias; it is due to a duplication at 17p11.2 leading to PMP22 overexpression. 20976668

2011
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
CUI: C0030554
Disease: Paresthesia
Paresthesia 		0.410 Biomarker CTD_human Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatment. 12427913

2002
Entrez Id: 5376
Gene Symbol: PMP22
PMP22
CUI: C0030554
Disease: Paresthesia
Paresthesia 		0.410 Biomarker HPO