IGLON5, IgLON family member 5, 402665

N. diseases: 16; N. variants: 2
Disease: Autoimmune encephalopathy with parasomnia and obstructive sleep apnea ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4707562
Disease: Autoimmune encephalopathy with parasomnia and obstructive sleep apnea
Autoimmune encephalopathy with parasomnia and obstructive sleep apnea 		0.020 Biomarker disease BEFREE We here describe the first case of a patient with coexisting anti-IgLON5 as well as anti-γ-aminobutyric acid B (GABAB)-receptor antibodies and predominant clinical features of anti-IgLON5 disease. 31096519 2019
CUI: C4707562
Disease: Autoimmune encephalopathy with parasomnia and obstructive sleep apnea
Autoimmune encephalopathy with parasomnia and obstructive sleep apnea 		0.020 Biomarker disease BEFREE HEK293 cells expressing several deletion constructs of IgLON5 were used to determine the epitopes recognized by the serum of 15 patients with anti-IgLON5 syndrome. 27586161 2016