Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 GeneticVariation disease UNIPROT Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. 9924029 1999
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 GeneticVariation disease UNIPROT Phenotypic variability in a Spanish family with MNGIE. 12177387 2002
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 GeneticVariation disease CLINVAR Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). 19056268 2009
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.400 GeneticVariation disease CLINVAR
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.100 GeneticVariation disease CLINVAR Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). 19056268 2009
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 Biomarker disease GENOMICS_ENGLAND A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies. 25655951 2015
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 Biomarker disease CTD_human
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 Biomarker disease GENOMICS_ENGLAND Late-onset MNGIE due to partial loss of thymidine phosphorylase activity. 16178026 2005
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 Biomarker disease GENOMICS_ENGLAND An atlas of genetic influences on human blood metabolites. 24816252 2014
Entrez Id: 5428
Gene Symbol: POLG
POLG 		0.400 Biomarker disease CTD_human
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1). 19748572 2009
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome. 15781193 2005
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR MNGIE: diarrhea and leukoencephalopathy. 12084896 2002
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Late-onset MNGIE due to partial loss of thymidine phosphorylase activity. 16178026 2005
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). 19056268 2009
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients. 12529715 2003
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Poor Outcome in a Mitochondrial Neurogastrointestinal Encephalomyopathy Patient with a Novel TYMP Mutation: The Need for Early Diagnosis. 23341816 2012
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstruction. 19344718 2009
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. 21933806 2011
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes. 14720311 2004
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Biochemical abnormalities in a patient with thymidine phosphorylase deficiency with fatal outcome. 20151198 2010
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Phenotypic variability in a Spanish family with MNGIE. 12177387 2002
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. 10852545 2000
Entrez Id: 1890
Gene Symbol: TYMP
TYMP 		0.700 CausalMutation disease CLINVAR Mitochondrial neurogastrointestinal encephalomyopathy in three siblings: clinical, genetic and neuroradiological features. 17294068 2007