TRNW, tRNA, 4578

N. diseases: 188; N. variants: 7
Disease: Maternally Inherited Leigh Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931092
Disease: Maternally Inherited Leigh Syndrome
Maternally Inherited Leigh Syndrome 		0.300 GermlineCausalMutation disease ORPHANET Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNA(Trp) in patients with Leigh syndrome. 19349200 2009
CUI: C2931092
Disease: Maternally Inherited Leigh Syndrome
Maternally Inherited Leigh Syndrome 		0.300 GermlineCausalMutation disease ORPHANET Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene. 9266739 1997