Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 100505887
Gene Symbol: LINC01672
LINC01672
CUI: C0598106
Disease: Encephalomyelopathy
Encephalomyelopathy 		0.010 Biomarker BEFREE It is argued that this rare disease, since the princeps description in 1964 only reported in England (1986) and the U.S.A (1986), is most likely a singular type of mitochondrial encephalopathy: it is associated with Leber's optic atrophy, and the NMR changes observed have been signalled in other mitochondrial encephalomyelopathies, such as Leigh's disease and MELAS. 1880538

1991