Disease: EDICT syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3280392
Disease: EDICT syndrome
EDICT syndrome 		0.010 GeneticVariation disease BEFREE We report the refinement of the linkage region for keratoconus with cataract to an interval of approximately 5.5 Mb flanked by the MAN2C1 gene and the D15S211 marker on chromosome 15q. 16735990 2006