Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11160
Gene Symbol: ERLIN2
ERLIN2
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		0.110 GeneticVariation BEFREE SPG2/Proteolipid protein and SPG42/Connexin 47); (5) protein folding and ER-stress response (SPG6/NIPA1, SPG8/K1AA0196 (Strumpellin), SGP17/BSCL2 (Seipin), "mutilating sensory neuropathy with spastic paraplegia" owing to CcT5 mutation and presumably SPG18/ERLIN2); (6) corticospinal tract and other neurodevelopment (e.g. 23897027

2013
Entrez Id: 11160
Gene Symbol: ERLIN2
ERLIN2
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		0.110 Biomarker HPO