LITAF, lipopolysaccharide induced TNF factor, 9516

N. diseases: 59; N. variants: 19
Disease: Hereditary liability to pressure palsies ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		0.020 GeneticVariation disease BEFREE Overall, this study shows that the I92V LITAF sequence variant would be a good candidate for a biomarker in the case of the CMT1A/HNPP disorders. 25342198 2015
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		0.020 GeneticVariation disease BEFREE In our patients, early-onset HNPP was associated frequently with isoleucine92valine LITAF polymorphism. 24668782 2014