LARS1, leucyl-tRNA synthetase 1, 51520

N. diseases: 38; N. variants: 10
Disease: INFANTILE LIVER FAILURE SYNDROME 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3809522
Disease: INFANTILE LIVER FAILURE SYNDROME 1
INFANTILE LIVER FAILURE SYNDROME 1 		0.700 Biomarker disease GENOMICS_ENGLAND Identification of a mutation in LARS as a novel cause of infantile hepatopathy. 22607940 2012
CUI: C3809522
Disease: INFANTILE LIVER FAILURE SYNDROME 1
INFANTILE LIVER FAILURE SYNDROME 1 		0.700 GermlineCausalMutation disease ORPHANET Identification of a mutation in LARS as a novel cause of infantile hepatopathy. 22607940 2012
CUI: C3809522
Disease: INFANTILE LIVER FAILURE SYNDROME 1
INFANTILE LIVER FAILURE SYNDROME 1 		0.700 GeneticVariation disease UNIPROT Identification of a mutation in LARS as a novel cause of infantile hepatopathy. 22607940 2012
CUI: C3809522
Disease: INFANTILE LIVER FAILURE SYNDROME 1
INFANTILE LIVER FAILURE SYNDROME 1 		0.700 Biomarker disease CTD_human
CUI: C3809522
Disease: INFANTILE LIVER FAILURE SYNDROME 1
INFANTILE LIVER FAILURE SYNDROME 1 		0.700 CausalMutation disease CLINVAR