Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11222
Gene Symbol: MRPL3
MRPL3 		0.700 Biomarker disease GENOMICS_ENGLAND COXPD9 an Evolving Multisystem Disease; Congenital Lactic Acidosis, Sensorineural Hearing Loss, Hypertrophic Cardiomyopathy, Cirrhosis and Interstitial Nephritis. 27815843 2017
Entrez Id: 11222
Gene Symbol: MRPL3
MRPL3 		0.700 Biomarker disease GENOMICS_ENGLAND Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy. 21786366 2011
Entrez Id: 11222
Gene Symbol: MRPL3
MRPL3 		0.700 GeneticVariation disease UNIPROT Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy. 21786366 2011
Entrez Id: 11222
Gene Symbol: MRPL3
MRPL3 		0.700 GermlineCausalMutation disease ORPHANET Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy. 21786366 2011
Entrez Id: 11222
Gene Symbol: MRPL3
MRPL3 		0.700 Biomarker disease CTD_human
Entrez Id: 11222
Gene Symbol: MRPL3
MRPL3 		0.700 CausalMutation disease CLINVAR