Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome
0.010 GeneticVariation disease BEFREE This prompted reanalysis of the 5'-untranslated structure of the human RABGGTA gene in normal individuals and in patients with deficiencies of platelet-dense granules (alphadelta-SPD), alpha granules (alpha-SPD or gray platelet syndrome, GPS) or alpha plus dense granules (alphadelta-SPD). 11136552 2000