| ");
+printf("Disclaimer\n");
+printf(" \n");
+printf("Note: OMIM is intended for use primarily ");
+printf("by physicians and other professionals concerned with genetic disorders, ");
+printf("by genetics researchers, and by advanced students in science and medicine. ");
+printf("While the OMIM database is open to the public, users seeking information ");
+printf("about a personal medical or genetic condition are urged to consult with a ");
+printf("qualified physician for diagnosis and for answers to personal questions.\n \n");
+printf("Because many OMIM records refer to multiple gene names, or syndromes not ");
+printf("tightly mapped to individual genes, the associations in this track should ");
+printf("be treated with skepticism and any conclusions based on them should be ");
+printf("carefully scrutinized using independent resources.\n");
+printf(" \n");
+printf(" \n");
+printf(" \n");
+printf(" |