18015d0223dafa5a895098ccf89f5ca1f03c8742 abenetpa Wed Jun 17 13:18:14 2020 -0700 corrected OMIM track names refs #25682 diff --git src/hg/makeDb/trackDb/human/omimDescriptionText.html src/hg/makeDb/trackDb/human/omimDescriptionText.html index f7e23c8..0d9a0c9 100644 --- src/hg/makeDb/trackDb/human/omimDescriptionText.html +++ src/hg/makeDb/trackDb/human/omimDescriptionText.html @@ -1,51 +1,51 @@ <div class="warn-note" style="border: 2px solid #9e5900; padding: 5px 20px; background-color: #ffe9cc;"> <p><span style="font-weight: bold; color: #c70000;">NOTE:</span><br> OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions. Further, please be sure to click through to <a href = "http://omim.org" target="_blank">omim.org</a> for the very latest, as they are continually updating data.</p> <p><span style="font-weight: bold; color: #c70000;">NOTE ABOUT DOWNLOADS:</span><br> OMIM is the property of Johns Hopkins University and is not available for download or mirroring by any third party without their permission. Please see <a href= "http://omim.org/downloads/" target="_blank">OMIM</A> for downloads.</p> </div> <P>OMIM is a compendium of human genes and genetic phenotypes. The full-text, referenced overviews in OMIM contain information on all known Mendelian disorders and over 12,000 genes. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, under the direction of Dr. Ada Hamosh. This database was initiated in the early 1960s by Dr. Victor A. McKusick as a catalog of Mendelian traits and disorders, entitled Mendelian Inheritance in Man (MIM). </P> <P> The OMIM data are separated into three separate tracks: </P> -<P><B>OMIM Alleles</B> +<P><B>OMIM Alellic Variant Phenotypes (OMIM Alleles)</B> <BR> Variants in the OMIM database that have associated dbSNP identifiers. -<P><B>OMIM Genes</B> +<P><B>OMIM Gene Phenotypes (OMIM Genes)</B> <BR> The genomic positions of gene entries in the OMIM database. The coloring indicates the associated OMIM phenotype map key. </P> -<P><B>OMIM Phenotypes - Gene Unknown</B> +<P><B>OMIM Cytogenetic Loci Phenotypes - Gene Unknown (OMIM Cyto Loci)</B> <BR> Regions known to be associated with a phenotype, but for which no specific gene is known to be causative. This track also includes known multi-gene syndromes. </P> <HR>