Fig. 3
From: PhenoExam: gene set analyses through integration of different phenotype databases
False positive rate of phenotype (a) and disease (b) terms enrichment across varying gene set sizes (5, 10, 20, 40, 80, 160, 320, 640) per phenotype/disease database. As the simulation points out, CRB, HPO, MGD, are perfectly usable for any gene set size, CTD is recommended for gene set sizes over 10, PsyGeNET for 20, CGI, ClinGen and Uniprot for 40, Orphanet for 80 and GEL for gene set sizes over 180