Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Muscular Dystrophy, Facioscapulohumeral
0.010 GeneticVariation disease BEFREE To test this, we used fluorescence in situ hybridization probes with FSHD and control myoblasts to characterize the distal portion of 4q35.2 with respect to the following: intense staining with the chromatin dye 4',6-diamidino-2-phenylindole; association with constitutively heterochromatic foci; extent of binding of heterochromatin protein 1alpha; histone H3 methylation at lysine 9 and lysine 4; histone H4 lysine 8 acetylation; and replication timing within S-phase. 15138770 2004