Gene: DMPK ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1760
Gene Symbol: DMPK
DMPK 		0.110 GeneticVariation phenotype BEFREE Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting. 20346670 2010
Entrez Id: 1760
Gene Symbol: DMPK
DMPK 		0.110 Biomarker phenotype HPO